
Optical Isomerism and Chirality Quiz

Passage
•
Chemistry
•
12th Grade
•
Hard
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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