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प्रश्न
Complete the following reaction giving major products.
\[\ce{CH3 - CH = CH2 ->[HBr][peroxide] A ->[alc. KOH] B}\]
उत्तर
\[\ce{\underset{Propene}{CH3 - CH} = CH2 ->[HBr][Peroxide]\underset{\underset{\overset{(A)}{(major product)}}{1-Bromopropane}}{CH3CH2CH2Br} ->[Alc.KOH]\underset{\underset{(B)}{propene}}{CH3CH} = CH2}\]
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संबंधित प्रश्न
from the following pair would undergo SN2 faster from the other?
a. CH3CH2CH2I b. CH3CH2CH2Cl
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- 1-Bromopropane
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- 1-Bromo-2-methylpropane
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tert-Butyl bromide to isobutyl bromide
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\[\begin{array}{cc}
\ce{CH3}\phantom{.......}\\
|\phantom{.........}\\
\ce{CH3 - c - CH2 - Cl ->[Na/dry ether]}\\
|\phantom{.........}\\
\ce{CH3}\phantom{.......}
\end{array}\]
Discuss β - elimination reaction.
Define and explain the SN1 mechanism with a suitable example.
Give a reason for the following:
Ethoxy ethane with conc. HI at 373 K gives C2H5OH and CH3I but not CH3OH and C2H5I.
