Cis and Trans Isomerism Concepts

Cis and Trans Isomerism Concepts

Assessment

Interactive Video

Created by

Ethan Morris

Chemistry, Science

9th - 12th Grade

Hard

The video tutorial explains cis and trans isomers, highlighting their distinct physical properties such as dipole moments and boiling points. It discusses the energy barriers preventing free rotation in these isomers, contrasting them with ethane. The tutorial also covers different representations of isomers and provides guidance on identifying alkenes that can exhibit cis and trans isomerism.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the main difference between cis and trans isomers?

Cis isomers are always nonpolar, trans are always polar.

Cis isomers have groups on the same side, trans have them on opposite sides.

Cis isomers have higher melting points than trans isomers.

Cis isomers have groups on opposite sides, trans have them on the same side.

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why does the cis isomer have a higher boiling point than the trans isomer?

Because it is nonpolar.

Because it has a higher molecular weight.

Because it is polar and has a net dipole moment.

Because it has more hydrogen bonds.

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which of the following is true about the dipole moment of trans isomers?

They have a dipole moment of approximately three dbi.

They have a higher dipole moment than cis isomers.

They have a dipole moment only in polar solvents.

They always have a dipole moment of zero.

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the boiling point of the cis isomer mentioned in the video?

37 degrees Celsius

47.5 degrees Celsius

60 degrees Celsius

100 degrees Celsius

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is required to convert a trans isomer to a cis isomer?

Breaking the pi bond.

Adding more hydrogen atoms.

Breaking the sigma bond.

Increasing the temperature slightly.

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the energy barrier for rotation in ethane compared to cis and trans isomers?

The same in both.

Higher in ethane.

Lower in ethane.

Non-existent in ethane.

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

How can cis and trans isomers be represented using rings?

By using wedges and dashes to show direction.

By using different colors for each group.

By drawing them as linear structures.

By placing all groups in the same plane.

8.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In the context of cis and trans isomers, what does a wedge represent?

A group going into the page.

A group coming out of the page.

A group on the same plane as the page.

A group that is nonpolar.

9.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What determines if an alkene can show cis and trans isomerism?

The presence of a triple bond.

The presence of different groups on each carbon of the double bond.

The presence of identical groups on the same carbon.

The presence of a single bond.

10.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why can't an alkene with identical groups on the same carbon show cis and trans isomerism?

Because it lacks a double bond.

Because it has free rotation.

Because it doesn't have different groups on each carbon of the double bond.

Because it is always nonpolar.

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