Question Description
Read the passage given below and answer the following questions:Aryl halides are extremely less reactive towards nucleophilic substitution reactions due to the following reasons:(i) In haloarenes, the electron pairs on halogen atom are in conjugation with π-electrons of the ring.(ii) In haloalkane, the carbon atom attached to halogen is sp3 hybridised while in case of haloarene, the carbon atom attached to halogen is sp2 -hybridised.(iii) In case of haloarenes, the phenyl cation formed as a result of self-ionisation will not be stabilised by resonance.Q. Which of the following alkyl halides will undergoes SN1 reaction most readily?a)(CH3)3C—Fb)(CH3)3C—Clc)(CH3)3C—Brd)(CH3)3C—ICorrect answer is option 'D'. Can you explain this answer? for Class 12 2024 is part of Class 12 preparation. The Question and answers have been prepared
according to
the Class 12 exam syllabus. Information about Read the passage given below and answer the following questions:Aryl halides are extremely less reactive towards nucleophilic substitution reactions due to the following reasons:(i) In haloarenes, the electron pairs on halogen atom are in conjugation with π-electrons of the ring.(ii) In haloalkane, the carbon atom attached to halogen is sp3 hybridised while in case of haloarene, the carbon atom attached to halogen is sp2 -hybridised.(iii) In case of haloarenes, the phenyl cation formed as a result of self-ionisation will not be stabilised by resonance.Q. Which of the following alkyl halides will undergoes SN1 reaction most readily?a)(CH3)3C—Fb)(CH3)3C—Clc)(CH3)3C—Brd)(CH3)3C—ICorrect answer is option 'D'. Can you explain this answer? covers all topics & solutions for Class 12 2024 Exam.
Find important definitions, questions, meanings, examples, exercises and tests below for Read the passage given below and answer the following questions:Aryl halides are extremely less reactive towards nucleophilic substitution reactions due to the following reasons:(i) In haloarenes, the electron pairs on halogen atom are in conjugation with π-electrons of the ring.(ii) In haloalkane, the carbon atom attached to halogen is sp3 hybridised while in case of haloarene, the carbon atom attached to halogen is sp2 -hybridised.(iii) In case of haloarenes, the phenyl cation formed as a result of self-ionisation will not be stabilised by resonance.Q. Which of the following alkyl halides will undergoes SN1 reaction most readily?a)(CH3)3C—Fb)(CH3)3C—Clc)(CH3)3C—Brd)(CH3)3C—ICorrect answer is option 'D'. Can you explain this answer?.
Solutions for Read the passage given below and answer the following questions:Aryl halides are extremely less reactive towards nucleophilic substitution reactions due to the following reasons:(i) In haloarenes, the electron pairs on halogen atom are in conjugation with π-electrons of the ring.(ii) In haloalkane, the carbon atom attached to halogen is sp3 hybridised while in case of haloarene, the carbon atom attached to halogen is sp2 -hybridised.(iii) In case of haloarenes, the phenyl cation formed as a result of self-ionisation will not be stabilised by resonance.Q. Which of the following alkyl halides will undergoes SN1 reaction most readily?a)(CH3)3C—Fb)(CH3)3C—Clc)(CH3)3C—Brd)(CH3)3C—ICorrect answer is option 'D'. Can you explain this answer? in English & in Hindi are available as part of our courses for Class 12.
Download more important topics, notes, lectures and mock test series for Class 12 Exam by signing up for free.
Here you can find the meaning of Read the passage given below and answer the following questions:Aryl halides are extremely less reactive towards nucleophilic substitution reactions due to the following reasons:(i) In haloarenes, the electron pairs on halogen atom are in conjugation with π-electrons of the ring.(ii) In haloalkane, the carbon atom attached to halogen is sp3 hybridised while in case of haloarene, the carbon atom attached to halogen is sp2 -hybridised.(iii) In case of haloarenes, the phenyl cation formed as a result of self-ionisation will not be stabilised by resonance.Q. Which of the following alkyl halides will undergoes SN1 reaction most readily?a)(CH3)3C—Fb)(CH3)3C—Clc)(CH3)3C—Brd)(CH3)3C—ICorrect answer is option 'D'. Can you explain this answer? defined & explained in the simplest way possible. Besides giving the explanation of
Read the passage given below and answer the following questions:Aryl halides are extremely less reactive towards nucleophilic substitution reactions due to the following reasons:(i) In haloarenes, the electron pairs on halogen atom are in conjugation with π-electrons of the ring.(ii) In haloalkane, the carbon atom attached to halogen is sp3 hybridised while in case of haloarene, the carbon atom attached to halogen is sp2 -hybridised.(iii) In case of haloarenes, the phenyl cation formed as a result of self-ionisation will not be stabilised by resonance.Q. Which of the following alkyl halides will undergoes SN1 reaction most readily?a)(CH3)3C—Fb)(CH3)3C—Clc)(CH3)3C—Brd)(CH3)3C—ICorrect answer is option 'D'. Can you explain this answer?, a detailed solution for Read the passage given below and answer the following questions:Aryl halides are extremely less reactive towards nucleophilic substitution reactions due to the following reasons:(i) In haloarenes, the electron pairs on halogen atom are in conjugation with π-electrons of the ring.(ii) In haloalkane, the carbon atom attached to halogen is sp3 hybridised while in case of haloarene, the carbon atom attached to halogen is sp2 -hybridised.(iii) In case of haloarenes, the phenyl cation formed as a result of self-ionisation will not be stabilised by resonance.Q. Which of the following alkyl halides will undergoes SN1 reaction most readily?a)(CH3)3C—Fb)(CH3)3C—Clc)(CH3)3C—Brd)(CH3)3C—ICorrect answer is option 'D'. Can you explain this answer? has been provided alongside types of Read the passage given below and answer the following questions:Aryl halides are extremely less reactive towards nucleophilic substitution reactions due to the following reasons:(i) In haloarenes, the electron pairs on halogen atom are in conjugation with π-electrons of the ring.(ii) In haloalkane, the carbon atom attached to halogen is sp3 hybridised while in case of haloarene, the carbon atom attached to halogen is sp2 -hybridised.(iii) In case of haloarenes, the phenyl cation formed as a result of self-ionisation will not be stabilised by resonance.Q. Which of the following alkyl halides will undergoes SN1 reaction most readily?a)(CH3)3C—Fb)(CH3)3C—Clc)(CH3)3C—Brd)(CH3)3C—ICorrect answer is option 'D'. Can you explain this answer? theory, EduRev gives you an
ample number of questions to practice Read the passage given below and answer the following questions:Aryl halides are extremely less reactive towards nucleophilic substitution reactions due to the following reasons:(i) In haloarenes, the electron pairs on halogen atom are in conjugation with π-electrons of the ring.(ii) In haloalkane, the carbon atom attached to halogen is sp3 hybridised while in case of haloarene, the carbon atom attached to halogen is sp2 -hybridised.(iii) In case of haloarenes, the phenyl cation formed as a result of self-ionisation will not be stabilised by resonance.Q. Which of the following alkyl halides will undergoes SN1 reaction most readily?a)(CH3)3C—Fb)(CH3)3C—Clc)(CH3)3C—Brd)(CH3)3C—ICorrect answer is option 'D'. Can you explain this answer? tests, examples and also practice Class 12 tests.