मराठी

C–Cl bond length in chlorobenzene is shorter than C–Cl bond length in CH3–Cl.

Advertisements
Advertisements

प्रश्न

C–Cl bond length in chlorobenzene is shorter than C–Cl bond length in CH3–Cl.

लघु उत्तर
Advertisements

उत्तर

In chlorobenzene, the C−Cl bond gets partial double bond character because of the +M effect shown by the Cl group. Due to double bond character, the bond length decreases in chlorobenzene as compared to the normal CH3−Cl bond length. Therefore, the C–Cl bond length in chlorobenzene is shorter than the C–Cl bond length in CH3–Cl.

shaalaa.com
  या प्रश्नात किंवा उत्तरात काही त्रुटी आहे का?
2015-2016 (March) Delhi Set 3

व्हिडिओ ट्यूटोरियलVIEW ALL [1]

संबंधित प्रश्‍न

Which alkyl halide from the following pair would you expect to react more rapidly by an SN2 mechanism? Explain your answer.

CH3CH2CH2CH2Br or \[\begin{array}{cc}
\ce{CH3CH2CHCH3}\\
\phantom{.....}|\\
\phantom{.......}\ce{Br}\ 
\end{array}\]


Out of C6H5CH2Cl and C6H5CHClC6H5, which is more easily hydrolysed by aqueous KOH.


What happens when ethyl chloride is treated with aqueous KOH?


Which of the following is optically inactive?


Halogenation of alkanes is ____________.


The increasing order of reactivity towards SN1 mechanism is:

(I) \[\begin{array}{cc}
\ce{CH3-CH-CH2-CH3}\\
|\phantom{........}\\
\ce{CH3}\phantom{.....}
\end{array}\]

(II) CH3CH2CH2Cl

(III) P–CH3O–C6H4–CH2Cl


Which of the following statements are correct about this reaction?

(i) The given reaction follows SN2 mechanism.

(ii) (b) and (d) have opposite configuration.

(iii) (b) and (d) have same configuration.

(iv) The given reaction follows SN1 mechanism.


Compound ‘A’ with molecular formula \[\ce{C4H9Br}\] is treated with aq. \[\ce{KOH}\] solution. The rate of this reaction depends upon the concentration of the compound ‘A’ only. When another optically active isomer ‘B’ of this compound was treated with aq. \[\ce{KOH}\] solution, the rate of reaction was found to be dependent on concentration of compound and \[\ce{KOH}\] both.

(i) Write down the structural formula of both compounds ‘A’ and ‘B’.

(ii) Out of these two compounds, which one will be converted to the product with inverted configuration.


Identify the product in the following reaction: 


Assertion (A): undergoes SN2 reactions faster than .

Reason (R): Iodine is a better leaving group because of its large size.

In the light of the above statements, choose the correct answer from the options given below:


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×