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

Which of the compounds will react faster in SN1 reaction with the –OH ion? CHA3−CHA2−Cl or CA6HA5−CHA2−Cl

Advertisements
Advertisements

प्रश्न

Which of the compounds will react faster in SN1 reaction with the OH ion?

\[\ce{CH3-CH2-Cl}\] or \[\ce{C6H5-CH2-Cl}\]

टिप्पणी लिखिए
Advertisements

उत्तर

\[\ce{C6H5-CH2-Cl}\]

SN1 reaction proceeds through the formation of carbonation intermediate.

\[\ce{C6H5CH2Cl}\] readily undergoes ionization to give \[\ce{C6H5CH^{+}2}\] carbocation, which is stabilized by resonance.

On the other hand, \[\ce{CH3CH2Cl}\] does not undergo ionization to give \[\ce{CH3CH^{+}2}\] carbonation. Therefore, \[\ce{C6H5CH2Cl}\] reacts faster than \[\ce{CH3CH2Cl}\] with \[\ce{OH-}\] ion.

shaalaa.com
  क्या इस प्रश्न या उत्तर में कोई त्रुटि है?
अध्याय 10: Haloalkanes and Haloarenes - Exercises [पृष्ठ १४२]

APPEARS IN

एनसीईआरटी एक्झांप्लर Chemistry Exemplar [English] Class 12
अध्याय 10 Haloalkanes and Haloarenes
Exercises | Q III. 46. | पृष्ठ १४२

संबंधित प्रश्न

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


Write the structures of A, B and C in the following:


How will you bring about the following conversion?

Toluene to benzyl alcohol


The treatment of alkyl chlorides with aqueous KOH leads to the formation of alcohols but in the presence of alcoholic KOH, alkenes are major products. Explain.


In a coordination entity of the type [PtCl2(en)2]2+ which isomer will show optical isomerism?


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


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


Which among MeX, RCH2X, R2CHX and R3CX is most reactive towards SN2 reaction?


Which of the following is a chiral compound?


Which of the following alkyl halides will undergo SN1 reaction most readily?


Assertion: KCN reacts with methyl chloride to give methyl isocyanide.

Reason: CN is an ambident nucleophile.


Complete the following analogy:

Same molecular formula but different structures: A : : Non superimposable mirror images: B


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.


Elimination reactions (especially β-elimination) are as common as the nucleophilic substitution reaction in case of alkyl halides. Specify the reagents used in both cases.


Chlorination of alkanes is an example of


CCl4 is insoluble in water because:-


In which reaction mechanism carbocation is formed?


Convert bromoethane to propanamine.


Discuss SN2 mechanism of methyl bromide using aqueous KOH.


Which of the following reactions is an example of nucleophilic substitution reaction?


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×