Advertisements
Advertisements
प्रश्न
from the following pair would undergo SN2 faster from the other?
Advertisements
उत्तर
Compound (a) will undergo SN2 mechanism faster than (b).
Explanation:
- Sincey
is a primary halide it undergoes S2N reaction faster than 
. - Since iodine is a better leaving group than chloride, 1-iodo propane (CH3CH2CH2I) undergoes S2N reaction faster than l-chloropropane (CH3CH2CH2CI).
APPEARS IN
संबंधित प्रश्न
Complete the following reaction giving major products.
\[\begin{array}{cc}\ce{CH3 - CH = CH3 ->[Red P/Br2] A ->[Ag2O/H2O]B}\\|\phantom{.........................}\\
\ce{OH\phantom{.......................}}\end{array}\]
Complete the following reaction giving major products.
Name the reagent used to bring about the following conversion.
1-Chloropropane to 1-nitropropane
Convert the following:
Propene to propan-1-ol
Convert the following:
tert-Butyl bromide to isobutyl bromide
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.
Can it react by SN1 mechanism? Justify your answer.
Major product of the following reaction is _______________
\[\ce{CH3-CH2-Mg-Br + NH3 ->?}\]
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.
What is dehydrohalogenation? State the rule for the formation of the preferred product of dehydrohalogenation.
Which of the following is least reactive towards nucleophilic addition?
Dehydrohalogenation of an alkyl halide is ____________.
\[\ce{C6H5CH2Cl + KCN(alc) -> X + Y}\]
Compounds X and Y are ____________.
Identify 'B' in the following reaction.
\[\ce{2-Bromobutane ->[KOH alc.][\Delta] A ->[HI] B}\]
Write the product formed when alkyl halide reacts with silver nitrite.
Which of the following statements is incorrect regarding the dehydrohalogenation of alkenes?
Which among the following statements is not correct about SN2 reaction mechanism?
Observe the following and answer the question given below:
Can react by SN1 mechanism? Justify your answer.
Define and explain the SN1 mechanism with a suitable example.
Complete the reaction:
\[\ce{CH3CH2Cl ->[AgCN][alc.\Delta]}\] ?
Identify the chiral molecule from the following.
Complete the following reaction giving major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{...............}\\
|\phantom{..................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether]A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{.................}
\end{array}\]
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 of the following pair of compounds on heating gives butanenitrile?
Identify the substrate 'X' in the following reaction.
\[\ce{\underset{}{X + O2} ->[i) Co-naphtenate 423 K][ii) dil HClΔ] \underset{\underset{}{}}{Phenol + Acetone}}\]
