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प्रश्न
from the following pair would undergo SN2 faster from the other?
a. CH3CH2CH2I b. CH3CH2CH2Cl
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उत्तर
Compound (a) will undergo SN2 mechanism faster than (b).
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संबंधित प्रश्न
Complete the following reaction giving major products.
\[\ce{CH3 - CH = CH2 ->[HBr][peroxide] A ->[alc. KOH] B}\]
Complete the following reaction giving major product.
\[\begin{array}{cc}\ce{CH3\phantom{................}}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3\phantom{................}}
\end{array}\]
Name the reagent used to bring about the following conversion.
1-Chloropropane to 1-nitropropane
Name the reagent used to bring about the following conversion.
Chlorobenzene to biphenyl
Give reasons:
Haloarenes are less reactive than haloalkanes.
Convert the following:
Ethanol to propane nitrile
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’.
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 aqueous alkaline hydrolysis of tert. butyl bromide.
Which of the following is a primary halide?
Which of the following is least reactive towards nucleophilic addition?
Nitroalkanes are obtained in laboratory from primary or secondary alkyl halides by the action of ______.
\[\ce{C6H5CH2Cl + KCN(alc) -> X + Y}\]
Compounds X and Y are ____________.
Which of the following is FALSE regarding SN2 reaction mechanism?
Convert the following.
p-Nitrochlorobenzene to p-nitrophenol
Which of the following statements is incorrect regarding the dehydrohalogenation of alkenes?
Which among the following statements is not correct about SN2 reaction mechanism?
Complete the following reactions giving a major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{..................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{..................}\\
\ce{CH3}\phantom{................}
\end{array}\]
Observe the following and answer the questions given below:
Name the type of halogen derivative.
Discuss β - elimination reaction.
Identify the chiral molecule from the following.
Complete the following reaction giving major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl->[Na/ dry ether]A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{................}\\
\end{array}\]
Which among the following is NOT benzylic halide?
Which of the following reagent is used for conversion of alkyl halide into nitrile?
