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Chapter 8: Q.31 (page 326)

Rank the following alkenes in order of increasing stability:

Short Answer

Expert verified

The stability of the alkenes are mentioned below:

Step by step solution

01

Identification of the double-bonded carbons

The double bonds are identified first.

Representation of the double bond

02

Classification based on substitution

Structure A is disubstituted. It is monosubstituted for B and trisubstituted for C.

Representation of the alkyl substituents

03

Stability based on the number of substitutions present

More the count of substitutions, more will be the alkene stability because, with the increase of substitution, +I effect of the alkyl groups increase the stability of the system.

So the mentioned alkenes are ranked in the following:

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Most popular questions from this chapter

Does cis-or trans-1-bromo-4-tert-butylcylohexane react faster in an E2 reaction?

What alkene is the major product formed from each alkyl halide in an E1 reaction?

a.

b.

c.

Draw the products in each reaction.

a.

b.

c.

d.

Given that an E2 reaction proceeds with anti periplanar stereochemistry, draw the products of each elimination. The alkyl halides in (a) and (b) are diastereomers of each other. How are the products of these two reactions related? Recall from Section 3.2A that -C6H5is a phenyl group, a benzene ring bonded to another group.

a.

b.

Draw an E1 mechanism for the following reaction. Draw the structure of the transition state for each step.
See all solutions

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