ORG CHEM CONNECT CARD
ORG CHEM CONNECT CARD
6th Edition
ISBN: 9781264860746
Author: SMITH
Publisher: MCG
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Chapter 7, Problem 63P
Interpretation Introduction

(a)

Interpretation: The given compounds A, B and C are to be arranged in order of increasing SN2 reactivity.

Concept introduction: An alkyl halide is classified as 1°, 2° or 3° when a halogen atom is bonded to primary, secondary or tertiary carbon atom of a hydrocarbon chain, respectively. A primary, secondary and tertiary carbon atom is bonded to one, two and three other carbon atoms, respectively. The order of increasing reactivity of alkyl halide towards SN2 reaction is vinyl<3°<2°<1°.

Interpretation Introduction

(b)

Interpretation: The given compounds A, B and C are to be arranged in order of increasing SN1 reactivity.

Concept introduction: In SN1 reaction mechanism, the removal of halide from alkyl halide leads to the formation of carbocation. The order of increasing stability of carbocation is vinyl<1°<2°<3°.

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(a) Rank A, B, and C in order of increasing SN2 reactivity. (b) Rank A, B, and C in order of increasing SN1 reactivity.
(a) Rank the following carbocations in order of increasing electrophilicity (1 = lowest electrophilicity, 4 = highest electrophilicity). (b) Rank the following 1,1-halomethylcyclopentanes in order of reactivity in an SN1 reaction (1 = lowest reactivity, 4 = highest reactivity. CH3 CI B with SNI, nor reactive means more stable (c) Rank the following species in terms of increasing nucleophilicity in an SN2 reaction in a po aprotic solvent (1 = lowest nucleophilicity, 4 = highest nucleophilicity).
(a) Draw all products formed by treatment of each dibromide (A and B) with one equivalent of NaNH2. (b) Label pairs of diastereomers and constitutional isomers. H Br H Br CH3 CH3 Br H H Br A

Chapter 7 Solutions

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