ORGANIC CHEM BUNDLE >BI<
ORGANIC CHEM BUNDLE >BI<
10th Edition
ISBN: 9781260719567
Author: Carey
Publisher: MCG
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Chapter 13, Problem 58P
Interpretation Introduction

Interpretation:

The mechanism for the conversion of hexamethylbenzene to compound B by directly inferring the structure of A is to be suggested.

Concept introduction:

In Friedel-Crafts reaction, the reaction of alkyl halides with benzene in the presence of aluminum chloride takes place to give alkylbenzenes.

The electrophile in Friedel-Crafts alkylation is the alkyl cation. The alkyl cation is generated by treating an alkyl chloride with aluminum chloride.

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On being heated with a solution of sodium ethoxide in ethanol, compound A (C7H15Br) produced a mixture of two alkenes B and C, each of which had the molecular formula C7H14. Catalytic hydrogenation of major isomer B or minor isomer C gave only 3-ethylpentane. Suggest structures and mechanisms for compounds A, B, and C consistent with these observations.
Compound A has the molecular formula C14H25Br and was obtained by reaction of sodium acetylide (HC≡CNa) )with 1,12-dibromododecane. On treatment of compound A with sodium amide, it was converted to compound B (C14H24). Ozonolysis of compound B gave the diacid HO2C(CH2)12CO2H. Catalytic hydrogenation of compound B over Lindlar palladium gave compound C (C14H26), while hydrogenation over platinum gave compound D (C14H28). Sodium-ammonia reduction of compound B gave compound E (C14H26). Both C and E yielded O═CH(CH2)12CH═O on ozonolysis. Assign structures to compound A through E so as to be consistent with the observed transformations.
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Chapter 13 Solutions

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