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🧪 Chemistry  ·  Organic Chemistry: Basic Principles and Techniques  ·  NEET & JEE

Which carbocation undergoes maximum hyperconjugation?

Answer: Tertiary.

  • A Methyl
  • B Primary
  • C Secondary
  • D Tertiary

Correct answer: D. Tertiary

Explanation: Tertiary carbocations have the maximum number of adjacent C-H bonds for hyperconjugation.

cis isomerClHClHsame side(Cl groups together)trans isomerClHHClopposite sides(Cl groups apart)

Geometric (cis-trans) isomers of 1,2-dichloroethene differ only in the relative arrangement of groups across the rigid C=C double bond.

Concept context

General Organic Chemistry covers the rules behind all organic reactions. Covers inductive effect, resonance, hyperconjugation, types of reactions (substitution, addition, elimination), and isomerism including optical and geometric forms.

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