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प्रश्न
Propane nitrile can be prepared by heating ____________
विकल्प
ethyl bromide with alcoholic KCN
propyl bromide with alcoholic KCN
ethyl bromide with alcoholic AgCN
propyl bromide with alcoholic AgCN
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उत्तर
ethyl bromide with alcoholic KCN
Explanation:
\[\ce{\underset{\text{Ethyl bromide}}{CH3CH2Br}->[Alc.KCN,\Delta][-H2O]\underset{\text{Propane nitrile}}{CH3CH2CN}}\]
APPEARS IN
संबंधित प्रश्न
from the following pair would undergo SN2 faster from the other?
a. CH3CH2CH2I b. CH3CH2CH2Cl
Give reasons:
Haloarenes are less reactive than haloalkanes.
Distinguish between SN1 and SN2 mechanism of substitution reaction.
Convert the following:
Ethanol to propane nitrile
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\[\ce{Isopropyl alcohol ->[\triangle][PBr3] A ->[][NH3 excess] B}\]
Observe the following and answer the question given below.

Comment on the bond length of C–X bond in it.
The following will react faster by SN1 mechanism
Which of the following is least reactive towards SN1 reactions?
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\[\ce{\underset{Ethyl bromide}{C2H5Br} + \underset{(aq.)}{KOH} ->[\Delta] \underset{Ethyl alcohol}{C2H5OH} + KBr}\]
Which of the following is a WRONG statement?
Which of the following is least reactive towards nucleophilic addition?
Nitroalkanes are obtained in laboratory from primary or secondary alkyl halides by the action of ______.
Which of the following carbocation is the most stable?
Identify major product 'B' in the following reaction.
\[\ce{But-1-ene ->[HBr][Peroxide] A ->[AgCN][\Delta] B}\]
What is the major product obtained in the sulphonation of chlorobenzene with concentrated sulphuric acid?
Which among the following statements is not correct about SN2 reaction mechanism?
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Complete the following reactions giving a major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{..................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{..................}\\
\ce{CH3}\phantom{................}
\end{array}\]
Observe the following and answer the question given below:

Comment on the bond length of C-X bond in it.
Discuss β - elimination reaction.
Define and explain the SN1 mechanism with a suitable example.
Complete the following reaction giving major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{...............}\\
|\phantom{..................}\\
\ce{CH3 - C - CH2 - Cl->[Na/dry ether]A}\\
|\phantom{..................}\\
\ce{CH3}\phantom{...............}\\
\end{array}\]
What is the action of following on ethyl bromide?
alcoholic sodium hydroxide
Complete the reaction:
\[\ce{CH3CH2Cl ->[AgCN][alc.\Delta]}\] ?
Complete the following reaction giving major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{..................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether]A}\\
|\phantom{..................}\\
\ce{CH3}\phantom{................}
\end{array}\]
Complete the following reaction giving major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl->[Na/ dry ether]A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{................}\\
\end{array}\]
Complete the following reaction giving major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{................}\\
\end{array}\]
