Elimination reaction of 2-Bromo-pentane to form pent-2-ene is: (a) β-Elimination reaction (b) Follows Zaitsev rule (c) Dehydrohalogenation reaction (d) Dehydration…

Elimination reaction of 2-Bromo-pentane to form pent-2-ene is: (a) $\beta$-Elimination reaction (b) Follows Zaitsev rule (c) Dehydrohalogenation reaction (d) Dehydration reaction
A (a), (c), (d)
B (b), (c), (d)
C (a), (b), (d)
D (a), (b), (c)

Detailed Solution

$CH_3-CH(Br)-CH_2-CH_2-CH_3 \xrightarrow{base} CH_3-CH=CH-CH_2-CH_3$ A $\beta$-hydrogen is abstracted, so it is a $\beta$-elimination reaction. The more substituted alkene (pent-2-ene) is formed, so it follows Zaitsev's rule. H and Br are removed, so it is a dehydrohalogenation reaction (not dehydration). So (a), (b) and (c) are correct.

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