English

From the following pair would undergo SN2 faster from the other? - Chemistry

Advertisements
Advertisements

Question

from the following pair would undergo SN2 faster from the other?

  1.    
One Line Answer
Advertisements

Solution

Compound (a) will undergo SN2 mechanism faster than (b).

Explanation:

  1. Sincey  is a primary halide it undergoes S2N reaction faster than .
  2. Since iodine is a better leaving group than chloride, 1-iodo propane (CH3CH2CH2I) undergoes S2N reaction faster than l-chloropropane (CH3CH2CH2CI).
shaalaa.com
Chemical Properties of Halogen Derivatives
  Is there an error in this question or solution?
Chapter 10: Halogen Derivatives - Exercises [Page 232]

APPEARS IN

Balbharati Chemistry [English] Standard 12 Maharashtra State Board
Chapter 10 Halogen Derivatives
Exercises | Q 2. iv. a. | Page 232

RELATED QUESTIONS

Complete the following reaction giving major products.

\[\ce{CH3 - CH = CH2 ->[HBr][peroxide] A ->[alc. KOH] B}\]


Complete the following reaction giving major products.

\[\begin{array}{cc}\ce{CH3 - CH = CH3 ->[Red P/Br2] A ->[Ag2O/H2O]B}\\|\phantom{.........................}\\
\ce{OH\phantom{.......................}}\end{array}\]


Name the reagent used to bring about the following conversion.

Bromoethane to ethoxyethane


Give reasons:

Haloarenes are less reactive than haloalkanes.


Distinguish between SN1 and SN2 mechanism of substitution reaction.


Convert the following:

Propene to propan-1-ol


Convert the following:

Benzyl alcohol to benzyl cyanide


Convert the following:

tert-Butyl bromide to isobutyl bromide


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'.

\[\ce{Isopropyl alcohol ->[\triangle][PBr3] A ->[][NH3 excess] B}\]


Observe the following and answer the question given below.

Can it react by SN1 mechanism? Justify your answer.


Propane nitrile can be prepared by heating ____________


The following will react faster by SN1 mechanism


Explain primary benzylic halide shows higher reactivity by SN1 mechanism than other primary alkyl halide.


The least reactive towards nucleophilic addition reactions is ____________.


Nitroalkanes are obtained in laboratory from primary or secondary alkyl halides by the action of ______.


Which one is most reactive towards nucleophilic addition reaction?


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 ____________.


Convert the following.

p-Nitrochlorobenzene to p-nitrophenol


The order of reactivity of the given haloalkanes towards nucleophiles is:


Explain the dehydrohalogenation reaction of 2-chlorobutane.


Complete the following reaction giving major products.

\[\begin{array}{cc}
\ce{CH3}\phantom{.......}\\
|\phantom{.........}\\
\ce{CH3 - c - CH2 - Cl ->[Na/dry ether]}\\
|\phantom{.........}\\
\ce{CH3}\phantom{.......}
\end{array}\]


Complete the following reactions giving a major product.

\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{..................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{..................}\\
\ce{CH3}\phantom{................}
\end{array}\]


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.


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 of the following reagent is used for conversion of alkyl halide into nitrile?


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×