EBK ORGANIC CHEMISTRY
EBK ORGANIC CHEMISTRY
6th Edition
ISBN: 8220103151757
Author: LOUDON
Publisher: MAC HIGHER
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Chapter 14, Problem 14.40AP
Interpretation Introduction

(a)

Interpretation:

The mechanism of reduction from 1alkynes to alkenes and its acidity are to be stated.

Concept introduction:

The compounds that contain carbon and hydrogen atoms are known as hydrocarbon compounds. These compounds originate from plants and animals. These are also known as organic compounds. There are two classes of hydrocarbon compounds which are saturated and unsaturated hydrocarbons. Unsaturated hydrocarbon compound are of two types alkenes and alkynes. The alkene contains a double bond between two carbon atoms. The alkynes contain a triple bond between two carbon atoms and follow general formula CnH2n-2. For example, HCCH. It is the smallest member of the alkynes class of compounds. The name of the alkyne compounds ends with suffix yne.

Interpretation Introduction

(b)

Interpretation:

The reason for complete conversion of 1alkynes into alkenes when (NH4)2SO4 is added is to be explained.

Concept introduction:

The compounds that contain carbon and hydrogen atoms are known as hydrocarbon compounds. These compounds originate from plants and animals. These are also known as organic compounds. There are two classes of hydrocarbon compounds which are Saturated and unsaturated hydrocarbons. Unsaturated hydrocarbon compound are of two types alkenes and alkynes. The alkene contains a double bond between two carbon atoms. The alkynes contains a triple bond between two carbon atoms and follow general formula CnH2n-2. For example, HCCH. It is the smallest member of the alkynes class of compounds. The name of the alkyne compounds ends with suffix yne.

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Draw the organic product obtained by hydroboration-oxidation of each of the following alkenes: (a) trans-2-pentene, (b) 2-tert-butyl-3,3-dimethyl-1- butene, and (c) 1-methylcyclohexene. Having done this, draw the product of the acid-catalyzed hydration of these same alkenes. How do the reaction products differ?
Q2. Consider the nucleophilic substitution reaction between 3-chloro-3-methylpentane and the hydroxide ion: CI x + OH (a) Is the alkyl halide 1°, 2° or 3°? (b) Will the nucleophilic substitution reaction be S₁1 or S№2? (c) Give the substitution mechanism showing all full and partial positive and negative charges, electron movements using curved arrows.
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