Label each pair of alkenes as constitutional isomers, stereoisomers, or identical.

a.

b.

c.

d.

Short Answer

Expert verified

For a. the pairs are constitutional isomers.

For b. the pairs are stereoisomers.

For c. the pairs are stereoisomers.

For d. the pairs are stereoisomers.

Step by step solution

01

Constitutional isomers, stereoisomers, and identical structures

  • Constitutional isomers are molecules having the same molecular formula, but the difference lies in bonding and molecular structure.These structures differ due to different orientations of the carbon atoms.
  • Stereoisomers isomers are isomers with same molecular formula. Their structures are the same but with different spatial arrangements.They are two kinds – cis/Z and trans/E.
  • Identical structures are those structures upon rotation resemble the same structure as its counterpart.
02

Identification of the double bond

The double-bonded carbons are identified first.

Representation of the double bond

03

Identification based on definitions

Based on the definition it is found that in the case of (a) constitutional isomers are present since the molecular formula is the same, but the position of the double bond is different.

For (b), (c) and (d) the high priority groups are lying in the opposite directions, hence they are considered to be stereoisomers.

For a. the pairs are constitutional isomers.

Pair of constitutional isomers

For b. the pairs are stereoisomers.

Pairs of stereoisomers

For c. the pairs are stereoisomers.

Pairs of stereoisomers

For d. the pairs are stereoisomers.

Pairs of stereoisomers

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

What alkenes are formed from each alkyl halide by an E1 reaction? Use the Zaitsev rule to predict the major product.

a.

b.

Draw the structure of a dihalide that could be used to prepare each alkyne. There may be more than one possible dihalide.

a.

b.

c.

For which reaction mechanisms—SN1,SN2,E1, or E2—are each of the following statements true? A statement may be true for one or more mechanisms.

a. The mechanism involves carbocation intermediates.

b. The mechanism has two steps.

c. The reaction rate increases with better leaving groups.

d. The reaction rate increases when the solvent is changed from CH3OHto localid="1648646954099" (CH3)2SO.

e. The reaction rate depends on the concentration of the alkyl halide only.

f. The mechanism is concerted.

g. The reaction of localid="1648646960420" CH3CH2Brwith NaOH occurs by this mechanism.

h. Racemization at a stereogenic center occurs.

i. Tertiary (3°) alkyl halides react faster than 2° or 1° alkyl halides.

j. The reaction follows a second-order rate equation.

Consider the following E2 reaction.

a. Draw the by-products of the reaction and use curved arrows to show the movement of

electrons.

b. What happens to the reaction rate with each of the following changes? [1] The solvent is changed to DMF. [2] The concentration of -OC(CH3)3is decreased. [3] The base is changed to localid="1648628375469" OH-. [4] The halide is changed to localid="1648628387551" CH3CH2CH2CH2CH(Br)CH3[5] The leaving group is changed to localid="1648628394364" I.

Draw all constitutional isomers formed in each elimination reaction. Label the mechanism as E2 or E1.

a.

b.

c.

d.

e.

f.

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free