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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
from the following pair would undergo SN2 faster from the other?
Arrange the following in the increasing order of boiling points.
- 1-Bromopropane
- 2- Bromopropane
- 1- Bromobutane
- 1-Bromo-2-methylpropane
Distinguish between SN1 and SN2 mechanism of substitution reaction.
Convert the following:
Propene to propan-1-ol
HCl is added to a hydrocarbon ‘A’ \[\ce{(C4H8)}\] to give a compound ‘B’ which on hydrolysis with aqueous alkali forms tertiary alcohol ‘C’ \[\ce{(C4H10O)}\]. Identify ‘A’ ,‘B’ and ‘C’.
Nucleophilic substitution reaction of 2, 4-dinitrochlorobenzene is faster than p-nitrochlorobenzene. Give reason.
Explain primary benzylic halide shows higher reactivity by SN1 mechanism than other primary alkyl halide.
In alkaline hydrolysis of tertiary butyl bromide, ____________.
Nitroalkanes are obtained in laboratory from primary or secondary alkyl halides by the action of ______.
How many metameric ethers are represented by the molecular formula C4H10O?
Which one is most reactive towards nucleophilic addition reaction?
\[\ce{C6H5CH2Cl + KCN(alc) -> X + Y}\]
Compounds X and Y are ____________.
Which of the following is FALSE regarding SN2 reaction mechanism?
Identify 'B' in the following reaction.
\[\ce{2-Bromobutane ->[KOH alc.][\Delta] A ->[HI] B}\]
Convert the following.
p-Nitrochlorobenzene to p-nitrophenol
The major product formed when 2-bromobutane is treated with alcoholic KOH is ______.
Explain the dehydrohalogenation reaction of 2-chlorobutane.
Complete the following reaction giving major products.
\[\begin{array}{cc}
\ce{CH3}\phantom{.......}\\
|\phantom{.........}\\
\ce{CH3 - c - CH2 - Cl ->[Na/dry ether]}\\
|\phantom{.........}\\
\ce{CH3}\phantom{.......}
\end{array}\]
Observe the following and answer the question given below:
Can react by SN1 mechanism? Justify your answer.
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.
\[\begin{array}{cc}
\ce{CH3}\phantom{...............}\\
|\phantom{..................}\\
\ce{CH3 - C - CH2 - Cl->[Na/dry ether]A}\\
|\phantom{..................}\\
\ce{CH3}\phantom{...............}\\
\end{array}\]
Give a reason for the following:
Ethoxy ethane with conc. HI at 373 K gives C2H5OH and CH3I but not CH3OH and C2H5I.
Which of the following pair of compounds on heating gives butanenitrile?
Which of the following reagent is used for conversion of alkyl halide into nitrile?
