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

Ethylene chloride and ethylidene chloride are isomers. Identify the correct statements. (i) Both the compounds form same product on treatment with alcoholic KOH. (ii) Both the compounds form

Advertisements
Advertisements

प्रश्न

Ethylene chloride and ethylidene chloride are isomers. Identify the correct statements.

(i) Both the compounds form same product on treatment with alcoholic KOH.

(ii) Both the compounds form same product on treatment with aq.NaOH.

(iii) Both the compounds form same product on reduction.

(iv) Both the compounds are optically active.

टीपा लिहा
Advertisements

उत्तर

(i) Both the compounds form same product on treatment with alcoholic KOH.

(iii) Both the compounds form same product on reduction.

Explanation:

\[\ce{\underset{(ethylidence chloride)}{H3C - CHCl2}}\]  and \[\begin{array}{cc}
\phantom{}\ce{H2C - CH2}\phantom{}\\
\phantom{}|\phantom{....}|\\
\phantom{.}\ce{\underset{(ethylene dichloride)}{\phantom{}Cl\phantom{...}Cl}}\phantom{}
\end{array}\]  are isomers.

(i) They give ethyne on treatment with alcoholic KOH.

\[\ce{CH3CHCl2 ->[alc][KOH] CH ≡ CH + 2KCl + 2H2O}\]

\[\ce{Cl - CH2 - CH2 - Cl ->[alc.KOH] CH ≡ CH + 2KCl + H2O}\]

(ii) On reduction with Zn dust in alcohol they give ethylene.

\[\ce{CH3CHCl2 + Zn ->[CH3OH] CH2 ≡ CH}\]

\[\ce{Cl - CH2 - CH2 - Cl + Zn ->[CH3OH] CH2 = CH2}\]

shaalaa.com
  या प्रश्नात किंवा उत्तरात काही त्रुटी आहे का?
पाठ 10: Haloalkanes and Haloarenes - Exercises [पृष्ठ १४१]

APPEARS IN

एनसीईआरटी एक्झांप्लर Chemistry Exemplar [English] Class 12
पाठ 10 Haloalkanes and Haloarenes
Exercises | Q II. 38. | पृष्ठ १४१

संबंधित प्रश्‍न

Write the structure of an isomer of compound C4H9Br which is most reactive towards SN1 reaction


Which would undergo SN1 reaction faster in the following pair and why?


Write the main products when methyl chloride is treated with AgCN.


Out of , which is more reactive towards SN1 reaction and why?


In the following pair of halogen compounds, which compound undergoes a faster SN1 reaction?


In the following pair of halogen compounds, which compound undergoes a faster SN1 reaction?


Write the structure of the major organic product in the following reaction:

\[\ce{CH3CH2Br + KCN ->[aq{.} ethanol]}\]


AgCN reacts with haloalkanes to form isocyanide. Haloalkanes react with KCN to form alkyl cyanides as the main product. Why?


Which compound in the following pair reacts faster in SN2 reaction with OH?

  1. CH3Br or CH3
  2. CH3Cl, (CH3)3CCl

Arrange the following organic compounds in descending order of their reactivity towards SN1 reaction.

C6H5CH2Br, C6H5CH(C6H5)Br, C6H5CH(CH3)Br, C6H5C(CH3)(C6H5)Br


Most reactive halide towards SN1 reaction is ____________.


Optically active isomers but not mirror images are called ____________.


SN1 reaction of alkyl halides lead to ___________.


The decreasing order of reactivity of the following compounds towards nucleophilic substitution (SN2) is ______.






Complete the reaction with the main product formed:


Convert bromoethane to propanamine.


The correct order of increasing reactivity of

C-X bond towards nucleophile in the following compounds is:


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:


The compound that will undergo SN1 reaction with the fastest rate is:


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×