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Solutions For Conversions in Organic Chemistry

The document provides a list of chemical reactions and the products that result from each reaction. There are over 50 entries that map starting materials to products through common organic reactions like alkylation, oxidation, reduction, hydrolysis, and others.

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NIMISH MUTYAPU
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31 views1 page

Solutions For Conversions in Organic Chemistry

The document provides a list of chemical reactions and the products that result from each reaction. There are over 50 entries that map starting materials to products through common organic reactions like alkylation, oxidation, reduction, hydrolysis, and others.

Uploaded by

NIMISH MUTYAPU
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd
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Solutions to the Conversions

A H2/ Pd/BaSO4 /Quinoline ( Lindlar catalyst) N Friedel Crafts alkylaton


CH3Cl : Methyl carbocation, (Electrophile)
B Ethene O Fuming sulphuric acid ( oleum,H2S2O7), Electrophile is SO3
C HBr P Br2 / AlBr3 : Electrophile is Bromonium ion, Br+
D Aq.KOH Q Friedel Crafts acylation, Ethanoyl chloride (acetyl chloride),
Ethanoyl (acetyl) carbocation, (Electrophile)
E Alc.KOH R Aniline
F Sodium ethoxide, (CH3CH2ONa)Williamson S Benzene diazonium chloride
synthesis
G O3/ Zn-H2O T Cu2Cl2/HCl; Sandmeyer reaction
H AgNO2 U Cu/HCl; Gatterman reaction
I Br2 / CCl4 V KI
J Alcoholic KOH W HBF4 / Heat : Balz Schiemann reaction
K NaNH2 / Mineral oil X CuCN/KCN
L Red hot iron tube,873K Y H3PO2
M Conc.HNO3/Conc and H2SO4: Electrophile is Z H2O ( Steam)
Nitronium ion,

1 KMnO4 /KOH and heat 28 CH3-CH2-CN (Propanenitrile)


2 Chromic acid 29 Propanamide
3 CrO2Cl2 /CS2 and H3O+ (Etards oxidation) 30 Propanoic acid
4 CrO3 / Ac2O and H3O+ 31 Propanoyl chloride
5 Zn-Hg /HCl (Clemmensen reduction) 32 Cl2 /Red P (Hell Volhard Zelinsky (HVZ) reaction)
6 NH2-NH2 , KOH/Ethylene glycol/Heat ( Wolf- 33 H2/Pd/BaSO4 (Rosenmund reduction)
Kishner reduction)
7 NaOH and CO2/H+ (Kolbe’s reaction) 34 LiAlH4 or NaHB4 or H2 / Ni or Pt or Pd
8 H3PO2 35 Propene
9 CHCl3/NaOH and H+ (Reimer-Tiemann 36 Propan-1-ol
reaction)
10 1,4-Benzoquinone 37 Br2/NaOH; (Hoffmann bromamide reaction
11 Cl2/UV/500K 38 CHCl3/KOH; (Carbylamine reaction)
12 Cl2/Anhydrous AlCl3/Dark/Cold 39 Zn/HCl or PCl3 or PCl5 or Red P/X2 or SOCl2
13 Benzaldehyde 40 Zn /HCl or Zn-Cu/ Ethanol or
Zn /Acetic acid or LiAlH4
14 Conc.Alkali 41 Ph-Br and Na/Dry ether (Wurtz -Fittig reaction)
15 Cold conc.H2SO4 42 CrO3 / Aq.H2SO4 ( Jones reagent) or pyridinium chlorochromate
(PCC) or PDC ( Pyridinium dichromate)
16 Cold, dil. Aq. KMnO4 (Baeyer’s reagent) 43 PhMgBr
17 Hg2+/H+ 44 I2/KOH ( Haloform reaction)
18 Acetaldehyde 45 HNO3, KMnO4, K2Cr2O7, or mild oxidizing agents like Tollens’
reagent and Fehlings’ reagents
19 Disodium acetylide 46 Dil.Alkali ( Aldol condensation)
20 But-2-yne 47 Na or NaOH or NaHCO3
21 Li or Na / Liq.NH3 48 Methane
22 CH3-I 49 Ethane (Kolbes electrolysis)
23 CH3-CH2-OH 50 Ethyl acetate (Fischer esterification
24 Ethyl ethanoate 51 Acetaldehyde oxime
25 Ethane 52 Zn / Ethyl alcohol
26 NaI (Finkelstein reaction) 53 1,1-Dibromoethane
27 AgF or Hg2F2 or CoF2 or SbF (Swarts reaction) 54 Acetaldehyde

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