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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.
\[\begin{array}{cc}\ce{CH3 - CH = CH3 ->[Red P/Br2] A ->[Ag2O/H2O]B}\\|\phantom{.........................}\\
\ce{OH\phantom{.......................}}\end{array}\]
Give reasons:
Haloarenes are less reactive than haloalkanes.
Propane nitrile can be prepared by heating ____________
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. Aryl halides are less reactive than alkyl halides towards nucleophilic substitution reactions.
Explain primary benzylic halide shows higher reactivity by SN1 mechanism than other primary alkyl halide.
Explain the factors affecting SN1 and SN2 mechanism.
Explain aqueous alkaline hydrolysis of tert. butyl bromide.
Which of the following is a primary halide?
Which of the following is least reactive towards SN1 reactions?
Dehydrohalogenation of an alkyl halide is ____________.
\[\ce{C6H5CH2Cl + KCN(alc) -> X + Y}\]
Compounds X and Y are ____________.
Which of the following carbocation is the most stable?
Write the product formed when alkyl halide reacts with silver nitrite.
The order of reactivities of the following alkyl halides for an SN2 reaction is ______.
Which of the following statements is incorrect regarding the dehydrohalogenation of alkenes?
Which among the following statements is not correct about SN2 reaction mechanism?
With which halogen the reactions, of alkanes are explosive?
Observe the following and answer the question given below:
Can react by SN1 mechanism? Justify your answer.
Complete the following reactions giving major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{.................}
\end{array}\]
What is the action of following on ethyl bromide?
alcoholic sodium hydroxide
Identify the substrate 'X' in the following reaction.
\[\ce{\underset{}{X + O2} ->[i) Co-naphtenate 423 K][ii) dil HClΔ] \underset{\underset{}{}}{Phenol + Acetone}}\]
Which among the following is NOT benzylic halide?
Which of the following reagent is used for conversion of alkyl halide into nitrile?
