Organic Chemistry - Standalone book
Organic Chemistry - Standalone book
10th Edition
ISBN: 9780073511214
Author: Francis A Carey Dr., Robert M. Giuliano
Publisher: McGraw-Hill Education
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Chapter 9.13, Problem 14P
Interpretation Introduction

Interpretation:

The ozonolysis of hydrocarbon having the molecular formula C16H26 gives CH3(CH2)4CO2H and HO2CCH2CH2CO2H as the only product, a reasonable structure for the hydrocarbon is to be suggested.

Concept Introduction:

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Ozonolysis of alkynes cleaves the triple bond producing carboxylic acids.

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Each of the triple bonded carbon atoms changes to carboxyl carbon.

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In case of terminal alkynes, one of the products is carbonic acid which dissociates into carbon dioxide and water.

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(a) Tsomane and Nyiko were given a task of synthesising methylenecyclohexane 2. After a brief discussion with each other, Tsomane proposed Method A to synthesise 2 from cyclohexanone 1 while Nyiko proposed Method B that started from hydroxymethylcyclohexane 3. Each student believed that their proposed method is better than the other. (Scheme below) (1) Ph Ph 8*8 Ph THF A 1 Santande B H₂SO4 100 °C 3 OH Using curly arrows, provide full mechanistic details accounting how methylenecyclohexane 2 was synthesised according to both Methods A and B.
We have a hydrocarbon, C16H26.  The compound has two triple bonds and the acids produced by ozonolysis are CH3(CH2)4CO2H and H2OCCH2CO2H.  What is a likely structure for this hydrocarbon?
Identify (A) in the following reaction. 2H2 Pt (A) KMNO4 Warm conc. || С — С — о—н |CO,H + HO CO2H cis-cyclo hexane 1,2-dicarboxylic acid (a) (b) (c) (d)

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Organic Chemistry - Standalone book

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