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प्रश्न
Complete the reaction:
\[\ce{CH3CH2Cl ->[AgCN][alc.\Delta]}\] ?
उत्तर
\[\ce{\underset{(Ethyl chloride)}{CH3CH2Cl} ->[AgCN][alc.\Delta] \underset{(Ethyl isocyanide)}{CH3 - CH2 - NC}}\]
APPEARS IN
संबंधित प्रश्न
from the following pair would undergo SN2 faster from the other?
a. 
b. 
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
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’.
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.
Name the type of halogen derivative.
Observe the following and answer the question given below.
Comment on the bond length of C–X bond in it.
The following will react faster by SN1 mechanism
Explain. Aryl halides are less reactive than alkyl halides towards nucleophilic substitution reactions.
Which of the following is a primary halide?
The following mechanism has been proposed for the reaction of NO2 with F2 to form NO2F:
\[\ce{NO2_{(g)} + F2_{(g)} -> NO2F_{(g)} + F_{(g)} (slow)}\]
\[\ce{F_{(g)} + NO2_{(g)} -> NO2F_{(g)} (fast)}\]
The order of the reaction with respect to NO2(g)
What type of hybridisation is present in carbocation formed during the alkaline hydrolysis of 1- bromo-1- phenyl ethane?
\[\ce{C6H5CH2Cl + KCN(alc) -> X + Y}\]
Compounds X and Y are ____________.
Which of the following carbocation is the most stable?
When C2H5Br is treated with excess of alc. NH3, the major product obtained is ____________.
The SN2 reaction of a compound containing an asymmetric carbon atom always gives ____________.
Identify major product 'B' in the following reaction.
\[\ce{But-1-ene ->[HBr][Peroxide] A ->[AgCN][\Delta] B}\]
The order of reactivities of the following alkyl halides for an SN2 reaction is ______.
Discuss β - elimination reaction.
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.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{.................}
\end{array}\]
Define and explain the SN1 mechanism with a suitable example.
Identify the chiral molecule from the following.
Give a reason for the following:
Ethoxy ethane with conc. HI at 373 K gives C2H5OH and CH3I but not CH3OH and C2H5I.
