Understanding Stereoisomerism in Alkenes

Understanding Stereoisomerism in Alkenes

Assessment

Interactive Video

Chemistry

10th - 12th Grade

Hard

Created by

Nancy Jackson

FREE Resource

5 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What type of hybridization do the carbons in a carbon-carbon double bond exhibit?

SP hybridization

SP2 hybridization

SP3 hybridization

No hybridization

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why is rotation restricted around a carbon-carbon double bond?

Because of the presence of a sigma bond

Due to the presence of a triple bond

Due to the lateral overlap of unhybridized p orbitals

Because of the presence of a single bond

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In the context of 2-butene, what does the term 'cis' refer to?

Hydrogen atoms on the same side of the double bond

Methyl groups on the same side of the double bond

Methyl groups on opposite sides of the double bond

Hydrogen atoms on opposite sides of the double bond

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which of the following statements is true about cis-trans isomerism?

It only applies to disubstituted alkenes.

It is not a type of stereoisomerism.

It is applicable when a carbon is attached to two identical groups.

It can apply to tri- and tetrasubstituted alkenes.

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

When is the cis-trans terminology not applicable?

When the molecule is a disubstituted alkene

When the double bond is part of a ring structure

When one of the carbons is attached to two identical groups

When one of the carbons is attached to two different groups