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Goc Worksheet

This document contains a chemistry worksheet with 15 multiple choice and assertion-reason type questions covering topics like resonance structures, functional groups, IUPAC naming conventions, isomerism, inductive effects, and more. Some key questions ask about which functional group has the highest priority in IUPAC nomenclature (-COOH), what type of isomerism is not found in alkenes (metamerism), and the electronic effects involved in hyperconjugation.

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139 views

Goc Worksheet

This document contains a chemistry worksheet with 15 multiple choice and assertion-reason type questions covering topics like resonance structures, functional groups, IUPAC naming conventions, isomerism, inductive effects, and more. Some key questions ask about which functional group has the highest priority in IUPAC nomenclature (-COOH), what type of isomerism is not found in alkenes (metamerism), and the electronic effects involved in hyperconjugation.

Uploaded by

deek_j
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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GRADE XI

CHEMISTRY
Ch- GOC
WORKSHEET

1. Which of the following cannot be represented by resonance structures?


a. Dimethyl ether
b. Nitrate anion
c. Carboxylate anion
d. Nitrobenzene
2. Inductive effect involves
a. displacement of σ electrons
b. delocalization of π electrons
c. delocalization of σ-electrons
d. displacement of π-electrons
3. Which of the following behaves both as a nucleophile and as an electrophile?
a. CH3C ≡ N
b. CH3OH
c. CH2 = CHCH3
d. CH3NH2
4. The kind of delocalization involving sigma bond in conjugation with pi electrons is called -
a. Inductive effect
b. Hyperconjugation effect
c. Electrometric effect
d. Mesomeric effect
5. The type of isomerism not found in alkenes is
a. Chain isomerism
b. Geometrical isomerism
c. Metamerism
d. Position isomerism

6. The correct decreasing order of priority for the functional groups of organic compounds in the IUPAC system
of nomenclature is:
a. –COOH, –SO3H, –CONH2, –CHO
b. –SO3H, –COOH, –CONH2, –CHO
c. –CHO, –COOH, –SO3H, –CONH2
d. –CONH2, –CHO, –SO3H, –COOH

7. The displacement of electrons in a multiple bond in the presence of attacking reagent is called -
a. Inductive effect
b. Electromeric effect
c. Resonance effect
d. Hyper conjugation effect

8. Write the IUPAC name of the following compound.

a. 4-methyl-4-ethyloctane
b. 4-Ethyl-4-methyloctane
c. 4-Ethyl-4-n-butylpentane
d. 2-Ethyl-2-butylpentane

9. Which of the following has least boiling point?


(a) n-hexane (b) n-pentane (c) 2-methyl butane (d) 2,2-dimethyl propane

10. Benzene molecule has


(a) 6 σ and 6  bonds
(b) 16 σ and 6  bonds
(c) 12 σ and 3  bonds
(d) 6 σ and 3  bonds

ASSERTION REASON TYPE


a. Assertion and reason are both correct statements and reason is correct explanation for assertion.
b. Assertion and reason are both correct statements but reason is not correct explanation for assertion.
c. Assertion is correct statement but reason is wrong statement.
d. Assertion is wrong statement but reason is correct statement.

11. Assertion: But-1-ene and 2-Methylprop-1-ene are position isomers.


Reason: Position isomers have same molecular formula but differ in the position of functional
groups.
12. Assertion: Tertiary carbocations are more stable than primary carbocations.
Reason: Hyperconjugation as well as inductive effect due to additional alkyl groups stabilize tertiary
carbocations.
13. Assertion: IUPAC name of compound CH3CH=CH–CHO is But-2-enal.
Reason: Functional group gets preference over multiple bond in IUPAC name of a compound.
14. Assertion: Energy of resonance hybrid is equal to the average of energies of all canonical forms.
Reason: Resonance hybrid cannot be presented by a single structure.\
15. Assertion (A): Toluene on Friedel Crafts methylation gives o– and p–xylene.
Reason (R): CH3-group bonded to benzene ring increases electron density at o– and p– position.

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