This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   Functional Groups in Organic Compounds  (workshop) University of Lincoln presentation
CLASSIFICATION OF HYDROCARBON COMPOUNDS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   HYDROCARBONS   contain only C and H atoms ALIPHATIC   hydrocarbons AROMATIC  Hydrocarbons must contain a  BENZENE ring UNSATURATED  hydrocarbons  contain at least 1 C–C multiple bond SATURATED   hydrocarbons  contain C–C and C–H  single bonds only (ALKANES) ALKENE  contains the  C=C functional group ALKYNE  contains the  C ≡C functional group
FUNCTIONAL GROUPS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   Name of functional group Functional group Example Endings on names Alcohol Ethanol -ol Aldehyde Ethanal (acetaldehyde) -al Ketone R ≠H Propanone (acetone) -one Carboxylic acid Ethanoic acid (acetic acid) -oic acid Ester R = alkyl Ethyl ethanoate (ethyl acetate) -oate Ether Diethyl ether Ether Amine Ethylamine -amine Amide Ethanamide (Acetamide) -amide Halogenoalkane X = F, Cl, Br, I Bromoethane Halo- Acid chloride Ethanoyl chloride -oyl chloride Nitrile Ethanenitrile -nitrile Nitro Nitromethane Nitro- Thiol Ethanethiol -thiol
FUNCTIONAL GROUPS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   PRIMARY (1 y ) ALCOHOL  R–CH 2 OH SECONDARY (2 y ) ALCOHOL R 2 –CHOH TERTIARY (3 y ) ALCOHOL R 3 –COH Where R– is any alkyl group Name of functional group Functional group Example Endings on names Alcohol Ethanol -ol Aldehyde Ethanal (acetaldehyde) -al Ketone R ≠H Propanone (acetone) -one Carboxylic acid Ethanoic acid (acetic acid) -oic acid Ester R = alkyl Ethyl ethanoate (ethyl acetate) -oate Ether Diethyl ether Ether Amine Ethylamine -amine Amide Ethanamide (Acetamide) -amide Halogenoalkane X = F, Cl, Br, I Bromoethane Halo- Acid chloride Ethanoyl chloride -oyl chloride Nitrile Ethanenitrile -nitrile Nitro Nitromethane Nitro- Thiol Ethanethiol -thiol
FUNCTIONAL GROUPS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   An acid is a proton (H+) donor Name of functional group Functional group Example Endings on names Alcohol Ethanol -ol Aldehyde Ethanal (acetaldehyde) -al Ketone R ≠H Propanone (acetone) -one Carboxylic acid Ethanoic acid (acetic acid) -oic acid Ester R = alkyl Ethyl ethanoate (ethyl acetate) -oate Ether Diethyl ether Ether Amine Ethylamine -amine Amide Ethanamide (Acetamide) -amide Halogenoalkane X = F, Cl, Br, I Bromoethane Halo- Acid chloride Ethanoyl chloride -oyl chloride Nitrile Ethanenitrile -nitrile Nitro Nitromethane Nitro- Thiol Ethanethiol -thiol
FUNCTIONAL GROUPS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   PRIMARY (1y) AMINE R–NH2 SECONDARY (2y) AMINE R2–NH TERTIARY (3y) AMINE R3–N Where R– is any alkyl group Name of functional group Functional group Example Endings on names Alcohol Ethanol -ol Aldehyde Ethanal (acetaldehyde) -al Ketone R ≠H Propanone (acetone) -one Carboxylic acid Ethanoic acid (acetic acid) -oic acid Ester R = alkyl Ethyl ethanoate (ethyl acetate) -oate Ether Diethyl ether Ether Amine Ethylamine -amine Amide Ethanamide (Acetamide) -amide Halogenoalkane X = F, Cl, Br, I Bromoethane Halo- Acid chloride Ethanoyl chloride -oyl chloride Nitrile Ethanenitrile -nitrile Nitro Nitromethane Nitro- Thiol Ethanethiol -thiol
Remember! GROUP 14 C arbon needs FOUR bonds 15 N itrogen needs THREE bonds 16 O xygen needs TWO bonds 17 F luorine needs ONE bond This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
Remember! By convention… This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   OH = = =
RECOGNISING FUNCTIONAL GROUPS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   Smelling of roses…
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   1 y  ALCOHOL  (–CH 2 OH)
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   1 y  ALCOHOL  (–CH 2 OH) ALKENE  (–C=C–)
Flower Scent – Freesia This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   Ketone (R–COR’)
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   Conjugated diene  (–C=C–C=C–) Ketone (R–COR’)
Pheromones – Honey bee This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   Pheromones are chemicals that carry messages
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   KETONE
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   Alkene Ketone
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   Carboxylic Acid (RCOOH) Alkene Ketone
AMPHETAMINES This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   AMPHETAMINE
AMPHETAMINES This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   1 y  AMINE (RNH 2 ) AMPHETAMINE
AMPHETAMINES This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   AROMATIC RING (Benzene) 1 y  AMINE (RNH 2 ) AMPHETAMINE
AMPHETAMINES This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   METHYLAMPHETAMINE
AMPHETAMINES This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   1H has been replaced with a –CH 3  (methyl) METHYLAMPHETAMINE
AMPHETAMINES This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   2 y  AMINE (RR’NH) 1H has been replaced with a –CH 3  (methyl) METHYLAMPHETAMINE
AMPHETAMINES This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   AROMATIC RING (Benzene) 2 y  AMINE (RR’NH) 1H has been replaced with a –CH 3  (methyl) METHYLAMPHETAMINE
ASPIRIN This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   CARBOXYLIC ACID (RCOOH) ASPIRIN
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   ESTER (RCOOR’) ASPIRIN CARBOXYLIC ACID (RCOOH)
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   AROMATIC RING (Benzene) ASPIRIN ESTER (RCOOR’) CARBOXYLIC ACID (RCOOH)
Bullet-proof vests and spider silk This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   KEVLAR (a polyamide)
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   AMIDE KEVLAR
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   AROMATIC RINGS KEVLAR AMIDE
Cat Nap (Octadec-9-eneamide) This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
Cat Nap (Octadec-9-eneamide) This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   ALKENE
Cat Nap (Octadec-9-eneamide) This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   ALKENE AMIDE
CANNABIS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
CANNABIS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   AROMATIC RING (Benzene)
CANNABIS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   AROMATIC RING (Benzene) AROMATIC ALCOHOL – A PHENOLIC GROUP
CANNABIS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   AROMATIC RING (Benzene) AROMATIC ALCOHOL – A PHENOLIC GROUP ALKENE
CANNABIS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   CYCLIC ETHER AROMATIC RING (Benzene) AROMATIC ALCOHOL – A PHENOLIC GROUP ALKENE
LSD (lysergic acid diethylamide) This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
LSD This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
LSD This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   DIETHYLAMIDE
LSD This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   3 Y  AMINE DIETHYLAMIDE
LSD This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   3 Y  AMINE DIETHYLAMIDE 2 Y  AMINE
LSD 3 Y  AMINE DIETHYLAMIDE 2 Y  AMINE This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   ALKENES
LSD 3 Y  AMINE DIETHYLAMIDE 2 Y  AMINE ALKENES This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   CONJUGATED DIENE
Identify FOUR functional groups in cocaine This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
COCAINE This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
COCAINE This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   2 ESTERS
COCAINE 2 ESTERS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   2 y  AMINE
COCAINE 2 ESTERS 2 y  AMINE This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   AROMATIC
Opium Morphine Codeine Thebaine This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
OPIUM This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   MORPHINE CODEINE THEBAINE HEROIN
Identify the functional groups in morphine This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
MORPHINE This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
MORPHINE This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   ALCOHOL
MORPHINE This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   PHENOL ALCOHOL
MORPHINE This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   CYCLIC ETHER PHENOL ALCOHOL
MORPHINE CYCLIC ETHER PHENOL ALCOHOL This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   AROMATIC
MORPHINE CYCLIC ETHER PHENOL ALCOHOL AROMATIC This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   3 Y  AMINE
MORPHINE This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   ALKENE CYCLIC ETHER PHENOL ALCOHOL AROMATIC 3 Y  AMINE
What’s the difference between morphine and codeine? This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   CODEINE MORPHINE
CODEINE MORPHINE This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   PHENOL
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   CODEINE MORPHINE PHENOL ETHER
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   CODEINE THEBAINE
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   CODEINE THEBAINE ALCOHOL
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   ETHER CODEINE THEBAINE ALCOHOL
HEROIN This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
HEROIN This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   2 ESTERS
Identify the functional groups in the ‘magic mushroom’ alkaloids This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
MAGIC MUSHROOMS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License   Acknowledgements JISC HEA Centre for Educational Research and Development School of natural and applied sciences School of Journalism SirenFM http://tango.freedesktop.org

More Related Content

PPT
Organic Chemistry: Classification of Organic Compounds
PPTX
Functional group of organic compounds
PPT
06 nomenclature _hydrocarbons__deriv._i
PPTX
Chapter 21.1 : Functional Groups and Classes of Organic Compounds
PPTX
Hydrocarbons and functional groups
PPTX
Functional groups
PPTX
1 hydrocarbons new
Organic Chemistry: Classification of Organic Compounds
Functional group of organic compounds
06 nomenclature _hydrocarbons__deriv._i
Chapter 21.1 : Functional Groups and Classes of Organic Compounds
Hydrocarbons and functional groups
Functional groups
1 hydrocarbons new

What's hot (20)

PDF
Organic chemistry nomenclature
PPT
Functional groups[1]
PPTX
Power Point On Hydrocarbon
PPT
Introduction to organic chemistry Foundation In science
PDF
Hydrocarbons
PPTX
Chemistry M5 Organic Chemistry
PDF
Alkane and cycloalkanes
PPT
General view of organic chemistry and iupac
PPTX
Naming of organic compounds ii, 23 (3)
PPT
Organic chemistry
DOCX
Alkanes
PPTX
Chapter 20.3 : Saturated and Unsaturated Hydrocarbons
PPTX
Nomenclature of Organic Compounds (IUPAC)
PPT
PPT
Esters (Functional Group)
PPT
Chapter 2 nomenclature of organic compounds
PPTX
Nomenclature of Carbon compounds
PDF
Nomenclature
PPTX
Chapter 3 Unsaturated Hydrocarbons
PDF
Functional groups
Organic chemistry nomenclature
Functional groups[1]
Power Point On Hydrocarbon
Introduction to organic chemistry Foundation In science
Hydrocarbons
Chemistry M5 Organic Chemistry
Alkane and cycloalkanes
General view of organic chemistry and iupac
Naming of organic compounds ii, 23 (3)
Organic chemistry
Alkanes
Chapter 20.3 : Saturated and Unsaturated Hydrocarbons
Nomenclature of Organic Compounds (IUPAC)
Esters (Functional Group)
Chapter 2 nomenclature of organic compounds
Nomenclature of Carbon compounds
Nomenclature
Chapter 3 Unsaturated Hydrocarbons
Functional groups
Ad

Viewers also liked (11)

PPT
Chemical Reactions: Kinetics
PDF
EPrints Analytics - Forensic Chemistry OER Course site, Feb/March 2011
PDF
ERIM, REDm-MED and Orbital (II)
PDF
Calculations using standard enthalpies of formation
PDF
Pencils And Pixels Overview Of Films
PDF
10 Steps To Sketching In The Landscape
PDF
Analytics for http://forensicchemistry.lincoln.ac.uk, Feb/March 2011
PDF
Structure of Matter seminar problems
PDF
Student as Producer stand
PPT
Chemical Reactions: Redox Reactions
PDF
ERIM, REDm-MED and Orbital
Chemical Reactions: Kinetics
EPrints Analytics - Forensic Chemistry OER Course site, Feb/March 2011
ERIM, REDm-MED and Orbital (II)
Calculations using standard enthalpies of formation
Pencils And Pixels Overview Of Films
10 Steps To Sketching In The Landscape
Analytics for http://forensicchemistry.lincoln.ac.uk, Feb/March 2011
Structure of Matter seminar problems
Student as Producer stand
Chemical Reactions: Redox Reactions
ERIM, REDm-MED and Orbital
Ad

Similar to Organic Chemistry: Classification of Organic Compounds: Seminar (20)

PPT
1. The most used Functional Groups in medicinal chemistry.ppt
PDF
Common Functional Groups in Organic Compounds
PPT
Pp organic 2
PPTX
Halides, alcohols
PPTX
New chm 152_unit_13_power_points-su13
PPT
Organicnomenclature
PDF
Alcohol, phenol and ether [autosaved]
PPTX
Ahl organic
PPTX
Introduction of Secondary metabolities (Volatile oil, Resin).pptx
PPT
Chapter_23_Power Point Presentation on Functional_Groups
PPT
Presentation of Functional Groups & Org Reactions.ppt
PPT
Optical isomers
PPTX
SIR Niamat
PDF
ORGCHEM-OLFU-SIR-TOFF.pptx.pdf
PPSX
Organic Chemistry: Introductory Topics
PPTX
Str and Uses_aldehyde and ketones.pptx
DOCX
Notes chapter 03
DOC
Chemistry - Microscale Preparation of Some Esters Lab
PDF
Unit 11
DOCX
Functional Groups a) what is an alcohol- how do you name alcohols- b).docx
1. The most used Functional Groups in medicinal chemistry.ppt
Common Functional Groups in Organic Compounds
Pp organic 2
Halides, alcohols
New chm 152_unit_13_power_points-su13
Organicnomenclature
Alcohol, phenol and ether [autosaved]
Ahl organic
Introduction of Secondary metabolities (Volatile oil, Resin).pptx
Chapter_23_Power Point Presentation on Functional_Groups
Presentation of Functional Groups & Org Reactions.ppt
Optical isomers
SIR Niamat
ORGCHEM-OLFU-SIR-TOFF.pptx.pdf
Organic Chemistry: Introductory Topics
Str and Uses_aldehyde and ketones.pptx
Notes chapter 03
Chemistry - Microscale Preparation of Some Esters Lab
Unit 11
Functional Groups a) what is an alcohol- how do you name alcohols- b).docx

More from ulcerd (15)

PPT
Chemical and Physical Properties: Practical Session
PPT
Chemical and Physical Properties: Isotopes and Forensic Science
PPT
Chemical and Physical Properties: Chemical vs. Physical Properties
PPT
Chemical Structure: Structure of Matter. Elements, Ions & Isotopes
PPT
Chemical Structure: Chemical Nomenclature. Inorganic Compounds
PPT
Chemical Structure: Chemical Bonding. Properties of Coordination Compounds
PPT
Chemical Structure: Chemical Bonding. Ionic, Metallic & Coordinate Bonds
PPT
Chemical Structure: Chemical Bonding. Polar Bonds
PPT
Chemical Structure: Chemical Bonding. Molecular Orbitals
PPT
Chemical Structure: Chemical Bonding. Homonuclear Covalent Bonds
PPT
Chemical Reactions: Thermochemistry
PPT
Chemical Reactions: pH Equilibria
PPT
Chemical and Physical Properties: Radioactivity & Radioisotopes
PPT
Chemical and Physical Properties: Isomerism
PPT
Chemical Structure: Structure of Matter. Atoms – the building blocks of matter
Chemical and Physical Properties: Practical Session
Chemical and Physical Properties: Isotopes and Forensic Science
Chemical and Physical Properties: Chemical vs. Physical Properties
Chemical Structure: Structure of Matter. Elements, Ions & Isotopes
Chemical Structure: Chemical Nomenclature. Inorganic Compounds
Chemical Structure: Chemical Bonding. Properties of Coordination Compounds
Chemical Structure: Chemical Bonding. Ionic, Metallic & Coordinate Bonds
Chemical Structure: Chemical Bonding. Polar Bonds
Chemical Structure: Chemical Bonding. Molecular Orbitals
Chemical Structure: Chemical Bonding. Homonuclear Covalent Bonds
Chemical Reactions: Thermochemistry
Chemical Reactions: pH Equilibria
Chemical and Physical Properties: Radioactivity & Radioisotopes
Chemical and Physical Properties: Isomerism
Chemical Structure: Structure of Matter. Atoms – the building blocks of matter

Recently uploaded (20)

PPTX
Virtual and Augmented Reality in Current Scenario
PDF
medical_surgical_nursing_10th_edition_ignatavicius_TEST_BANK_pdf.pdf
PPTX
TNA_Presentation-1-Final(SAVE)) (1).pptx
PPTX
A powerpoint presentation on the Revised K-10 Science Shaping Paper
PPTX
B.Sc. DS Unit 2 Software Engineering.pptx
PDF
Vision Prelims GS PYQ Analysis 2011-2022 www.upscpdf.com.pdf
PDF
IGGE1 Understanding the Self1234567891011
PDF
LDMMIA Reiki Yoga Finals Review Spring Summer
PDF
Uderstanding digital marketing and marketing stratergie for engaging the digi...
PDF
Hazard Identification & Risk Assessment .pdf
PPTX
Share_Module_2_Power_conflict_and_negotiation.pptx
PDF
Τίμαιος είναι φιλοσοφικός διάλογος του Πλάτωνα
PDF
HVAC Specification 2024 according to central public works department
PDF
ChatGPT for Dummies - Pam Baker Ccesa007.pdf
PDF
Trump Administration's workforce development strategy
PDF
David L Page_DCI Research Study Journey_how Methodology can inform one's prac...
PDF
A GUIDE TO GENETICS FOR UNDERGRADUATE MEDICAL STUDENTS
PDF
FOISHS ANNUAL IMPLEMENTATION PLAN 2025.pdf
PPTX
Computer Architecture Input Output Memory.pptx
PDF
1.3 FINAL REVISED K-10 PE and Health CG 2023 Grades 4-10 (1).pdf
Virtual and Augmented Reality in Current Scenario
medical_surgical_nursing_10th_edition_ignatavicius_TEST_BANK_pdf.pdf
TNA_Presentation-1-Final(SAVE)) (1).pptx
A powerpoint presentation on the Revised K-10 Science Shaping Paper
B.Sc. DS Unit 2 Software Engineering.pptx
Vision Prelims GS PYQ Analysis 2011-2022 www.upscpdf.com.pdf
IGGE1 Understanding the Self1234567891011
LDMMIA Reiki Yoga Finals Review Spring Summer
Uderstanding digital marketing and marketing stratergie for engaging the digi...
Hazard Identification & Risk Assessment .pdf
Share_Module_2_Power_conflict_and_negotiation.pptx
Τίμαιος είναι φιλοσοφικός διάλογος του Πλάτωνα
HVAC Specification 2024 according to central public works department
ChatGPT for Dummies - Pam Baker Ccesa007.pdf
Trump Administration's workforce development strategy
David L Page_DCI Research Study Journey_how Methodology can inform one's prac...
A GUIDE TO GENETICS FOR UNDERGRADUATE MEDICAL STUDENTS
FOISHS ANNUAL IMPLEMENTATION PLAN 2025.pdf
Computer Architecture Input Output Memory.pptx
1.3 FINAL REVISED K-10 PE and Health CG 2023 Grades 4-10 (1).pdf

Organic Chemistry: Classification of Organic Compounds: Seminar

  • 1. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License Functional Groups in Organic Compounds (workshop) University of Lincoln presentation
  • 2. CLASSIFICATION OF HYDROCARBON COMPOUNDS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License HYDROCARBONS contain only C and H atoms ALIPHATIC hydrocarbons AROMATIC Hydrocarbons must contain a BENZENE ring UNSATURATED hydrocarbons contain at least 1 C–C multiple bond SATURATED hydrocarbons contain C–C and C–H single bonds only (ALKANES) ALKENE contains the C=C functional group ALKYNE contains the C ≡C functional group
  • 3. FUNCTIONAL GROUPS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License Name of functional group Functional group Example Endings on names Alcohol Ethanol -ol Aldehyde Ethanal (acetaldehyde) -al Ketone R ≠H Propanone (acetone) -one Carboxylic acid Ethanoic acid (acetic acid) -oic acid Ester R = alkyl Ethyl ethanoate (ethyl acetate) -oate Ether Diethyl ether Ether Amine Ethylamine -amine Amide Ethanamide (Acetamide) -amide Halogenoalkane X = F, Cl, Br, I Bromoethane Halo- Acid chloride Ethanoyl chloride -oyl chloride Nitrile Ethanenitrile -nitrile Nitro Nitromethane Nitro- Thiol Ethanethiol -thiol
  • 4. FUNCTIONAL GROUPS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License PRIMARY (1 y ) ALCOHOL R–CH 2 OH SECONDARY (2 y ) ALCOHOL R 2 –CHOH TERTIARY (3 y ) ALCOHOL R 3 –COH Where R– is any alkyl group Name of functional group Functional group Example Endings on names Alcohol Ethanol -ol Aldehyde Ethanal (acetaldehyde) -al Ketone R ≠H Propanone (acetone) -one Carboxylic acid Ethanoic acid (acetic acid) -oic acid Ester R = alkyl Ethyl ethanoate (ethyl acetate) -oate Ether Diethyl ether Ether Amine Ethylamine -amine Amide Ethanamide (Acetamide) -amide Halogenoalkane X = F, Cl, Br, I Bromoethane Halo- Acid chloride Ethanoyl chloride -oyl chloride Nitrile Ethanenitrile -nitrile Nitro Nitromethane Nitro- Thiol Ethanethiol -thiol
  • 5. FUNCTIONAL GROUPS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License An acid is a proton (H+) donor Name of functional group Functional group Example Endings on names Alcohol Ethanol -ol Aldehyde Ethanal (acetaldehyde) -al Ketone R ≠H Propanone (acetone) -one Carboxylic acid Ethanoic acid (acetic acid) -oic acid Ester R = alkyl Ethyl ethanoate (ethyl acetate) -oate Ether Diethyl ether Ether Amine Ethylamine -amine Amide Ethanamide (Acetamide) -amide Halogenoalkane X = F, Cl, Br, I Bromoethane Halo- Acid chloride Ethanoyl chloride -oyl chloride Nitrile Ethanenitrile -nitrile Nitro Nitromethane Nitro- Thiol Ethanethiol -thiol
  • 6. FUNCTIONAL GROUPS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License PRIMARY (1y) AMINE R–NH2 SECONDARY (2y) AMINE R2–NH TERTIARY (3y) AMINE R3–N Where R– is any alkyl group Name of functional group Functional group Example Endings on names Alcohol Ethanol -ol Aldehyde Ethanal (acetaldehyde) -al Ketone R ≠H Propanone (acetone) -one Carboxylic acid Ethanoic acid (acetic acid) -oic acid Ester R = alkyl Ethyl ethanoate (ethyl acetate) -oate Ether Diethyl ether Ether Amine Ethylamine -amine Amide Ethanamide (Acetamide) -amide Halogenoalkane X = F, Cl, Br, I Bromoethane Halo- Acid chloride Ethanoyl chloride -oyl chloride Nitrile Ethanenitrile -nitrile Nitro Nitromethane Nitro- Thiol Ethanethiol -thiol
  • 7. Remember! GROUP 14 C arbon needs FOUR bonds 15 N itrogen needs THREE bonds 16 O xygen needs TWO bonds 17 F luorine needs ONE bond This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
  • 8. Remember! By convention… This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License OH = = =
  • 9. RECOGNISING FUNCTIONAL GROUPS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License Smelling of roses…
  • 10. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License 1 y ALCOHOL (–CH 2 OH)
  • 11. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License 1 y ALCOHOL (–CH 2 OH) ALKENE (–C=C–)
  • 12. Flower Scent – Freesia This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
  • 13. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License Ketone (R–COR’)
  • 14. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License Conjugated diene (–C=C–C=C–) Ketone (R–COR’)
  • 15. Pheromones – Honey bee This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License Pheromones are chemicals that carry messages
  • 16. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
  • 17. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License KETONE
  • 18. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License Alkene Ketone
  • 19. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License Carboxylic Acid (RCOOH) Alkene Ketone
  • 20. AMPHETAMINES This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License AMPHETAMINE
  • 21. AMPHETAMINES This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License 1 y AMINE (RNH 2 ) AMPHETAMINE
  • 22. AMPHETAMINES This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License AROMATIC RING (Benzene) 1 y AMINE (RNH 2 ) AMPHETAMINE
  • 23. AMPHETAMINES This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License METHYLAMPHETAMINE
  • 24. AMPHETAMINES This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License 1H has been replaced with a –CH 3 (methyl) METHYLAMPHETAMINE
  • 25. AMPHETAMINES This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License 2 y AMINE (RR’NH) 1H has been replaced with a –CH 3 (methyl) METHYLAMPHETAMINE
  • 26. AMPHETAMINES This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License AROMATIC RING (Benzene) 2 y AMINE (RR’NH) 1H has been replaced with a –CH 3 (methyl) METHYLAMPHETAMINE
  • 27. ASPIRIN This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
  • 28. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License CARBOXYLIC ACID (RCOOH) ASPIRIN
  • 29. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License ESTER (RCOOR’) ASPIRIN CARBOXYLIC ACID (RCOOH)
  • 30. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License AROMATIC RING (Benzene) ASPIRIN ESTER (RCOOR’) CARBOXYLIC ACID (RCOOH)
  • 31. Bullet-proof vests and spider silk This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
  • 32. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License KEVLAR (a polyamide)
  • 33. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License AMIDE KEVLAR
  • 34. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License AROMATIC RINGS KEVLAR AMIDE
  • 35. Cat Nap (Octadec-9-eneamide) This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
  • 36. Cat Nap (Octadec-9-eneamide) This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License ALKENE
  • 37. Cat Nap (Octadec-9-eneamide) This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License ALKENE AMIDE
  • 38. CANNABIS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
  • 39. CANNABIS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License AROMATIC RING (Benzene)
  • 40. CANNABIS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License AROMATIC RING (Benzene) AROMATIC ALCOHOL – A PHENOLIC GROUP
  • 41. CANNABIS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License AROMATIC RING (Benzene) AROMATIC ALCOHOL – A PHENOLIC GROUP ALKENE
  • 42. CANNABIS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License CYCLIC ETHER AROMATIC RING (Benzene) AROMATIC ALCOHOL – A PHENOLIC GROUP ALKENE
  • 43. LSD (lysergic acid diethylamide) This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
  • 44. LSD This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
  • 45. LSD This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License DIETHYLAMIDE
  • 46. LSD This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License 3 Y AMINE DIETHYLAMIDE
  • 47. LSD This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License 3 Y AMINE DIETHYLAMIDE 2 Y AMINE
  • 48. LSD 3 Y AMINE DIETHYLAMIDE 2 Y AMINE This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License ALKENES
  • 49. LSD 3 Y AMINE DIETHYLAMIDE 2 Y AMINE ALKENES This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License CONJUGATED DIENE
  • 50. Identify FOUR functional groups in cocaine This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
  • 51. COCAINE This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
  • 52. COCAINE This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License 2 ESTERS
  • 53. COCAINE 2 ESTERS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License 2 y AMINE
  • 54. COCAINE 2 ESTERS 2 y AMINE This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License AROMATIC
  • 55. Opium Morphine Codeine Thebaine This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
  • 56. OPIUM This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License MORPHINE CODEINE THEBAINE HEROIN
  • 57. Identify the functional groups in morphine This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
  • 58. MORPHINE This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
  • 59. MORPHINE This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License ALCOHOL
  • 60. MORPHINE This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License PHENOL ALCOHOL
  • 61. MORPHINE This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License CYCLIC ETHER PHENOL ALCOHOL
  • 62. MORPHINE CYCLIC ETHER PHENOL ALCOHOL This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License AROMATIC
  • 63. MORPHINE CYCLIC ETHER PHENOL ALCOHOL AROMATIC This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License 3 Y AMINE
  • 64. MORPHINE This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License ALKENE CYCLIC ETHER PHENOL ALCOHOL AROMATIC 3 Y AMINE
  • 65. What’s the difference between morphine and codeine? This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
  • 66. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License CODEINE MORPHINE
  • 67. CODEINE MORPHINE This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License PHENOL
  • 68. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License CODEINE MORPHINE PHENOL ETHER
  • 69. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License CODEINE THEBAINE
  • 70. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License CODEINE THEBAINE ALCOHOL
  • 71. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License ETHER CODEINE THEBAINE ALCOHOL
  • 72. HEROIN This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
  • 73. HEROIN This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License 2 ESTERS
  • 74. Identify the functional groups in the ‘magic mushroom’ alkaloids This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
  • 75. MAGIC MUSHROOMS This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
  • 76. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License Acknowledgements JISC HEA Centre for Educational Research and Development School of natural and applied sciences School of Journalism SirenFM http://tango.freedesktop.org

Editor's Notes

  • #32: Golden Orb Spider – spins a polyamide silk
  • #38: Chemical produced in sleep-deprived cats. Thought it might be good as a cure for insomnia
  • #57: Heroin is made from morphine, the main constituent of opium
  • #72: ALKENE GROUP HAS ALSO MOVED