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प्रश्न
Complete the reaction:
\[\ce{CH3CH2Cl ->[AgCN][alc.\Delta]}\] ?
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उत्तर
\[\ce{\underset{(Ethyl chloride)}{CH3CH2Cl} ->[AgCN][alc.\Delta] \underset{(Ethyl isocyanide)}{CH3 - CH2 - NC}}\]
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संबंधित प्रश्न
Complete the following reaction giving major products.
\[\begin{array}{cc}\ce{CH3 - CH = CH3 ->[Red P/Br2] A ->[Ag2O/H2O]B}\\|\phantom{.........................}\\
\ce{OH\phantom{.......................}}\end{array}\]
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 products.
Name the reagent used to bring about the following conversion.
1-Chloropropane to 1-nitropropane
Name the reagent used to bring about the following conversion.
Chlorobenzene to biphenyl
Convert the following:
Benzyl alcohol to benzyl cyanide
Convert the following:
Ethanol to propane nitrile
Complete the following reaction sequence by writing the structural formulae of the organic compound 'A', 'B' and 'C'.
\[\ce{2-Bromobutane->[Alc.KOH]A->[][Br2]B->[][NaNH2]C}\]
Observe the following and answer the question given below.
Can it react by SN1 mechanism? Justify your answer.
The following will react faster by SN1 mechanism
Write the correct order of increasing ease of dehydrohalogenation.
\[\ce{\underset{\text{(I)}}{CH3 - CH2 - CH2 - Cl}}\]
\[\ce{\underset{\text{(II)}}{CH3 - CH(Cl) - CH3}}\]
\[\begin{array}{cc}
\ce{CH3}\\
|\\
\ce{CH3-C-Cl}\phantom{...}\\
|\\
\ce{CH3}\\
\ce{(III)}
\end{array}\]
Explain the factors affecting SN1 and SN2 mechanism.
In alkaline hydrolysis of tertiary butyl bromide, ____________.
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Which one is most reactive towards nucleophilic addition reaction?
Which of the following carbocation is the most stable?
Which of the following is FALSE regarding SN2 reaction mechanism?
The SN2 reaction of a compound containing an asymmetric carbon atom always gives ____________.
The major product formed when 2-bromobutane is treated with alcoholic KOH is ______.
The order of reactivities of the following alkyl halides for an SN2 reaction is ______.
With which halogen the reactions, of alkanes are explosive?
The compound that reacts the fastest with sodium methoxide is ______.
Explain the dehydrohalogenation reaction of 2-chlorobutane.
Complete the following reaction giving major products.
\[\begin{array}{cc}
\ce{CH3}\phantom{.......}\\
|\phantom{.........}\\
\ce{CH3 - c - CH2 - Cl ->[Na/dry ether]}\\
|\phantom{.........}\\
\ce{CH3}\phantom{.......}
\end{array}\]
Complete the following reaction sequences by writing the structural formulae of the organic compounds 'A', 'B' and 'C'.
\[\ce{2-Bromobutan ->[alc. KOH] A ->[][Br2] B ->[][NANH2] C}\]
Complete the following reactions 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.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{..................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether]A}\\
|\phantom{..................}\\
\ce{CH3}\phantom{................}
\end{array}\]
