Optical Isomerism and Chirality Quiz

Optical Isomerism and Chirality Quiz

Assessment

Passage

Chemistry

12th Grade

Hard

Created by

Subash Teacher

FREE Resource

30 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the result of chirality in molecules with a single chiral centre?

Geometric isomerism

Optical isomerism

Structural isomerism

Positional isomerism

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

How can data on optical activity be used in organic chemistry?

To determine the boiling point of a compound

As evidence for SN1 and SN2 mechanisms

To identify the color of a compound

To measure the solubility of a compound

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What distinguishes structural isomers from other types of isomers?

They have the same connectivity of atoms but different spatial arrangements

They have different connectivity of atoms

They have the same physical properties

They are always geometric isomers

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which type of isomerism involves molecules that have the same connectivity but differ in the spatial arrangement of atoms?

Structural isomerism

Stereoisomerism

Geometric isomerism

Chain isomerism

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which of the following best defines isomers?

Molecules with the same molecular formula but different structural formulae.

Molecules with different molecular formulae but the same structure.

Molecules with the same structure and same molecular formula.

Molecules with different atoms and different structures.

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why can geometric isomers exist in molecules with C=C bonds?

Because the double bond can rotate freely.

Because the double bond cannot be rotated.

Because the single bond cannot be rotated.

Because the atoms are joined in a different order.

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which of the following is NOT a criterion for a molecule to exhibit E/Z isomerism?

The molecule must have a C=C double bond.

Each carbon in the double bond must be attached to two different groups.

The molecule must have a triple bond.

The double bond must be present.

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