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The reaction, CH₂ = CH-CH₃ + HBr → CH₃CHBr - CH₃ is
  • a)
    Nucleophilic addition
  • b)
    Electrophilic substitution
  • c)
    Electrophilic addition
  • d)
    Free radical addition
Correct answer is option 'C'. Can you explain this answer?
Verified Answer
The reaction, CH = CH-CH + HBr → CHCHBr - CH isa)Nucleophilic add...
Answer :
Addition of H−x(x→ Halogens ) on alkenes follows electrophilic addition mechanism.
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The reaction, CH = CH-CH + HBr → CHCHBr - CH isa)Nucleophilic add...
Electrophilic Addition
This reaction involves the addition of an electrophile (HBr) to a double bond (CH=CH-CH). The double bond acts as a nucleophile, attacking the electrophile to form a new bond. This type of reaction is known as electrophilic addition.

Mechanism:
1. The double bond in CH=CH-CH acts as a nucleophile and attacks the electrophile HBr.
2. The pi bond breaks as the nucleophile attacks, forming a carbocation intermediate.
3. The Br- ion then attacks the carbocation, forming the final product CHCHBr-CH.

Characteristics of Electrophilic Addition:
- Involves the addition of an electrophile to a double bond.
- Forms a carbocation intermediate.
- Typically occurs with alkenes or alkynes.
- Product is formed by addition of electrophile to the double bond.
In this reaction, the electrophile HBr adds to the double bond in CH=CH-CH, resulting in the formation of CHCHBr-CH. This reaction follows the characteristics of electrophilic addition, making option 'C' the correct answer.
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The reaction, CH = CH-CH + HBr → CHCHBr - CH isa)Nucleophilic additionb)Electrophilic substitutionc)Electrophilic additiond)Free radical additionCorrect answer is option 'C'. Can you explain this answer?
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