Given below are four compounds :
(a) n-propyl chloride
(b) iso-propyl chloride
(c) sec-butyl chloride
(d) neo-pentyl chloride
Percentage of carbon in the one which exhibits optical isomerism is :
- A
- B
- C
- D
Given below are four compounds :
(a) n-propyl chloride
(b) iso-propyl chloride
(c) sec-butyl chloride
(d) neo-pentyl chloride
Percentage of carbon in the one which exhibits optical isomerism is :
Correct answer:D
Standard Method
Given: Four compounds are listed: n-propyl chloride, iso-propyl chloride, sec-butyl chloride, and neo-pentyl chloride.
Find: The percentage of carbon in the compound that exhibits optical isomerism.
A compound shows optical isomerism when it contains a chiral carbon bonded to four different groups.
From the given compounds:
Therefore, the required compound is sec-butyl chloride with molecular formula .
Now calculate the mass percentage of carbon:
Mass of carbon:
Molar mass of :
So,
Rounding to the nearest integer:
Therefore, the correct option is D.
Identify the chiral compound first
Given: The four compounds are compared for optical isomerism.
Find: Which one is optically active and then its carbon percentage.
The key idea is that optical isomerism requires a carbon attached to four different substituents.
In sec-butyl chloride, the relevant carbon is bonded to:
Since all four groups are different, this carbon is chiral. The other listed chlorides do not contain such a carbon.
Hence the compound is sec-butyl chloride, .
Now compute carbon percentage using atomic masses , , and :
Thus the percentage of carbon is approximately , so the correct option is D.
Mistake: Assuming every secondary alkyl chloride shows optical isomerism. Why it is wrong: a chiral center requires four different groups on the carbon. What to do instead: check all four substituents explicitly before declaring the molecule optically active.
Mistake: Marking iso-propyl chloride as chiral. Why it is wrong: the central carbon is attached to two identical groups, so it is not a stereogenic center. What to do instead: look for repeated groups around the candidate carbon.
Mistake: Using the wrong molecular formula for sec-butyl chloride. Why it is wrong: an incorrect formula gives the wrong molar mass and wrong carbon percentage. What to do instead: write the structure carefully and count atoms to get .
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