मराठी
कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

(a) (b) (c)

Advertisements
Advertisements

प्रश्न

Arrange the following compounds in increasing order of rate of reaction towards nucleophilic substitution.

(a)
(b)
(c)

पर्याय

  • (a) < (b) < (c)

  • (a) < (c) < (b)

  • (c) < (b) < (a)

  • (b) < (c) < (a)

MCQ
Advertisements

उत्तर

(b) < (c) < (a)

Explanation:

The presence of electron releasing group at ortho- and para-positions decreases the reactivity of haloarenes. Because of the possible repulsion, it is less likely for the electron-rich nucleophile to approach electron-rich arenes. \[\ce{CH3}\] is an electron releasing group and is ortho and para - directors.

shaalaa.com
  या प्रश्नात किंवा उत्तरात काही त्रुटी आहे का?
पाठ 10: Haloalkanes and Haloarenes - Exercises [पृष्ठ १३९]

APPEARS IN

एनसीईआरटी एक्झांप्लर Chemistry Exemplar [English] Class 12
पाठ 10 Haloalkanes and Haloarenes
Exercises | Q I. 27. | पृष्ठ १३९

संबंधित प्रश्‍न

What happens when \[\ce{CH3 - Br}\] is treated with KCN?


Write the final product(s) in each of the following reactions:


The presence of nitro group (−NO2) at o/p positions increases the reactivity of haloarenes towards nucleophilic substitution reactions.


How the following conversion can be carried out?

Chlorobenzene to p-nitrophenol


What is Grignard reagent?


Write chemical equation in support of your answer. 
 Out of   Cl and  CH2- Cl,  which one is more reactive towards nucleophilic substitution reaction and why? 


Out of (CH3)3 C-Br and (CH3)3 C-I, which one is more reactive towards SN1 and why? 


Assertion: Presence of a nitro group at ortho or para position increases the reactivity of haloarenes towards nucleophilic substitution.

Reason: Nitro group, being an electron-withdrawing group decreases the electron density over the benzene ring.


Arrange the following compounds in increasing order of rate of reaction towards nucleophilic substitution.

(a)
(b)
(c)

Arrange the following compounds in increasing order of rate of reaction towards nucleophilic substitution.

(a)
(b)
(c)

Allyl chloride is hydrolysed more readily than n-propyl chloride. Why?


\[\ce{C6H12O6 ->[(Zymase)] A ->[NaOH][\Delta] B + CHI3}\]

The number of carbon atoms present in the product B is:


Assertion: Chlorobenzene is resistant to nucleophilic substitution reaction at room temperature.

Reason (R): C–Cl bond gets weaker due, to resonance.


Why haloarenes are not reactive towards nucleophilic substitution reaction? Give two reactions.


In the reaction, \[\mathrm{CH}_3\mathrm{C}\equiv\mathrm{\overline{C}Na}^++(\mathrm{CH}_3)_2\mathrm{CHCl}\to\] the product formed is ______.


Identify the final product [D] obtained in the following sequence of reactions.

\[\ce{CH3CHO \underset{ii) H2O+}{\overset{i) LiAlH4}{->}} [A] \underset{\triangle}{\overset{H2SO4}{->}} [B]}\]


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×