Advertisements
Advertisements
प्रश्न
Write the structure of the major product in each of the following reaction :
Advertisements
उत्तर
संबंधित प्रश्न
In the following pair of halogen compounds, which compound undergoes a faster SN1 reaction?
Out of C6H5CH2Cl and C6H5CHClC6H5, which is more easily hydrolysed by aqueous KOH.
Given reasons: SN1 reactions are accompanied by racemization in optically active alkyl halides.
Which one of the following halogen compounds is difficult to be hydrolysed by SN1 mechanism?
Identify X and Y in the following sequence:
\[\ce{C2H5Br ->[X] Product ->[Y] C3H7NH2}\]
Which of the following compound will undergo racemisation when reacts with aq. KOH?
(i)
(ii)
CH3CH2CH2Cl
(iii)
\[\begin{array}{cc}
\ce{CH3}\phantom{..}\\
|\phantom{....}\\
\ce{CH3-CH-CH2Cl}
\end{array}\]
(iv)
\[\begin{array}{cc}
\phantom{..}\ce{H}\\
\phantom{..}|\\
\ce{CH3-C-Cl}\\
\phantom{..}|\\
\phantom{.....}\ce{C2H5}
\end{array}\]
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 \[\ce{C6H5-CH2-Cl}\]
HCI, Major product ______.
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:
