English

Observe the following and answer the question given below. Comment on the bond length of C–X bond in it.

Advertisements
Advertisements

Question

Observe the following and answer the question given below.

Comment on the bond length of C–X bond in it.

One Line Answer
Advertisements

Solution

The bond length of C – X bond is expected to be shorter than C – X bond in haloalkanes.

shaalaa.com
  Is there an error in this question or solution?
Chapter 10: Halogen Derivatives - Exercises [Page 233]

APPEARS IN

Balbharati Chemistry [English] Standard 12 Maharashtra State Board
Chapter 10 Halogen Derivatives
Exercises | Q 7. iii. b. | Page 233

RELATED QUESTIONS

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

  1.    

Complete the following reaction giving major products.

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


Complete the following reaction giving major products.


Name the reagent used to bring about the following conversion.

Bromoethane to ethoxyethane


Name the reagent used to bring about the following conversion.

1-Chloropropane to 1-nitropropane


Give reasons:

Haloarenes are less reactive than haloalkanes.


Convert the following:

Benzyl alcohol to benzyl cyanide


Convert the following:

2-Chloropropane to propan-1-ol


Convert the following:

tert-Butyl bromide to isobutyl bromide


Observe the following and answer the question given below.

Can it react by SN1 mechanism? Justify your answer.


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.


Ethyl bromide undergoes the following reaction:

\[\ce{\underset{Ethyl bromide}{C2H5Br} + \underset{(aq.)}{KOH} ->[\Delta] \underset{Ethyl alcohol}{C2H5OH} + KBr}\]

Which of the following is a WRONG statement?


\[\ce{C6H5CH2Cl + KCN(alc) -> X + Y}\]

Compounds X and Y are ____________.


Which of the following carbocation is the most stable?


Identify 'B' in the following reaction.

\[\ce{2-Bromobutane ->[KOH alc.][\Delta] A ->[HI] B}\]


Which of the following statements is incorrect regarding the dehydrohalogenation of alkenes?


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


With which halogen the reactions, of alkanes are explosive?


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.

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


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?


Which among the following is NOT benzylic halide?


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


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×