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प्रश्न
Write the main products when methyl chloride is treated with AgCN.
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उत्तर
When methyl chloride is treated with AgCN, methyl cyanide is formed.
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संबंधित प्रश्न
Write the structure of the major organic product in the following reaction:
\[\ce{CH3CH(Br)CH2CH3 + NaOH ->[water]}\]
Which one of the following halogen compounds is difficult to be hydrolysed by SN1 mechanism?
Optically active isomers but not mirror images are called ____________.
The correct order of increasing the reactivity of C–X bond towards nucleophile in following compounds.
(I)
(II)
(CH3)3CCl
(III)
(CH3)2CHCl
(IV)
Assertion: KCN reacts with methyl chloride to give methyl isocyanide.
Reason: CN– is an ambident nucleophile.
Which of the compounds will react faster in SN1 reaction with the –OH ion?
\[\ce{CH3-CH2-Cl}\] or \[\ce{C6H5-CH2-Cl}\]
Write the structures and names of the compounds formed when compound ‘A’ with molecular formula, \[\ce{C7H8}\] is treated with \[\ce{Cl2}\] in the presence of \[\ce{FeCl3}\].
Give reason for the following:
The product formed during SN1 reaction is a racemic mixture.
Inversion of configuration occurs in ______.
Assertion (A): 
undergoes SN2 reactions faster than 
.
Reason (R): Iodine is a better leaving group because of its large size.
In the light of the above statements, choose the correct answer from the options given below:
