BPSC PGT Chemistry Important Questions: (Organic Chemistry)

BPSC PGT Chemistry Important Questions: (Organic Chemistry) – Isomerism

Home » BPSC PGT Chemistry » BPSC PGT Chemistry Important Questions: (Organic Chemistry) – Isomerism

1. A compound with the same molecular formula exists in two forms, one is alcohol and the other is Ether. What type of isomerism does it show?
a) metamerism
b) positional isomerism
c) functional isomerism
d) chain isomerism

Answer: c
Explanation: Functional isomerism occurs when compounds have the same molecular formula but different functional groups. For example, C₃H₆O can exist as an aldehyde or a ketone. Similarly, the given compound can exist as an alcohol or an ether, showing functional isomerism.

2. What is the specific rotation if its observed rotation is given as 3x, its length is given as x and density is given as 3/y?
a) 2y
b) 3y
c) y
d) 4y

Answer: c
Explanation: The specific rotation is given by the expression observed rotation/length X density, here as observed rotation is given as 3x and its length is given as x, while the density is 3/y, the specific rotation equals 3x/x(y/3) = y.

Thus, the specific rotation equals y.

3. Acetaldehyde and ethenol show ____________
a) stereoisomerism
b) metamerism
c) positional isomerism
d) tautomerism

Answer: d
Explanation: Acetaldehyde and ethenol show tautomerism, a special type of functional isomerism found in carbonyl compounds with an α-hydrogen atom. It involves the interconversion between the keto form and the enol form.

4. If a compound has 3 chiral carbons, what is the number of optically active isomers?
a) 9
b) 3
c) 4
d) 8

Answer: d
Explanation: The number of optically active isomers of a compound is calculated using the formula 2ⁿ, where n is the number of chiral carbons. Since this compound has 3 chiral carbons (n = 3), the total number of optically active isomers is 2³ = 8.

5. How many planes of symmetry does a meso compound have?
a) 2
b) 1
c) 3
d) 4

Answer: b
Explanation: A meso compound is one in which one half of the molecule is a mirror image of the other half. Such compounds usually contain two or more chiral centers and possess a plane of symmetry. Meso compounds are optically inactive because of internal compensation.

6. Enantiomers are the same as diastereomers.
a) true
b) false

Answer: b
Explanation: In optical isomerism, enantiomers are non-superimposable mirror images of each other, while diastereomers are also non-superimposable but are not mirror images. Diastereomers differ from each other in both physical and chemical properties.

7. The d-form is also known as ____________
a) rotatory
b) laevorotatory
c) dextrorotatory
d) l-form

Answer: c
Explanation: An isomer that rotates the plane of polarized light to the right (clockwise) is called dextrorotatory (d-form), while one that rotates it to the left (anticlockwise) is called laevorotatory (l-form).

8. Optical isomerism is a type of ____________
a) metamerism
b) stereoisomerism
c) geometrical isomerism
d) tautomerism

Answer: b
Explanation: Compounds with the same molecular formula but different spatial arrangements of atoms or groups are called stereoisomers, and this property is known as stereoisomerism. It is classified into three types: optical isomerism, geometrical isomerism, and conformational isomerism.

9. Which of the following is not a type of structural isomerism?
a) geometric isomerism
b) chain isomerism
c) metamerism
d) tautomerism

Answer: a
Explanation: Structural isomerism occurs when compounds have the same molecular formula but different structures. It is further classified into chain isomerism, position isomerism, functional isomerism, metamerism, and tautomerism. Hence, geometrical isomerism does not fall under structural isomerism.

10. 2-chloropropane and 1-chloropropane exhibit ____________ isomerism.
a) chain
b) position
c) functional
d) metamerism

Answer: b
Explanation: Compounds that share the same molecular formula but differ in the position of a functional group or substituent are called positional isomers, and this phenomenon is known as position isomerism. For example, 1-chloropropane and 2-chloropropane differ in the position of the chlorine atom; hence, they are positional isomers.

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