Question:

Observe the following reaction sequence (major product). \[ \mathrm{CH_3CH_2CH_2Br} \xrightarrow{\mathrm{HBr}} Y \xrightarrow[\text{major}]{\mathrm{alc.\ KOH}} Z \] Correct statement regarding \(Z\) is

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For alkenes, the number of hyperconjugative structures is approximately equal to the number of \(\alpha\)-hydrogen atoms attached to the carbon adjacent to the double bond.
Updated On: Jul 9, 2026
  • Number of \(\sigma\) bonds in it is two
  • Number of hyperconjugative resonance structures possible for it is 6
  • It does not exhibit cis-trans isomerism
  • It is the chain isomer of \(X\) \bigskip
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The Correct Option is B

Solution and Explanation

Step 1: Identify \(Y\). Addition of HBr to propene (Markovnikov addition) gives \[ Y=\mathrm{CH_3CHBrCH_3} \] (2-bromopropane).

Step 2:
Identify \(Z\). On treatment with alcoholic KOH, dehydrohalogenation occurs. \[ \mathrm{CH_3CHBrCH_3} \xrightarrow{\mathrm{alc.\ KOH}} \mathrm{CH_3CH=CH_2} \] Thus, \[ Z=\mathrm{CH_3CH=CH_2} \] (propene).

Step 3:
Analyse the options.
• Propene contains more than two \(\sigma\)-bonds. Hence incorrect.
• Propene has six \(\alpha\)-hydrogen atoms and therefore six hyperconjugative structures. \checkmark
• Propene cannot show cis-trans isomerism because one double-bonded carbon has two identical hydrogen atoms.
• Propene is not the chain isomer of \(X\).

Step 4:
Final conclusion. Hence, the correct statement is \[ \boxed{\text{Number of hyperconjugative resonance structures possible is }6.} \] Therefore, the correct option is \(\boxed{(B)}\).
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