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In nucleophilic substitution reactions, the reactivity of carbonyl compounds follows the order
- a)H₂C═O>R₂C═O>Ar₂C═O>RCHO>ArCHO
- b)H₂C═O>RCHO>ArCHO>R₂C═O>Ar₂C═0
- c)Ar₂C═O>R₂C═O>ArCHO>RCHO>H₂C═O
- d)ArCHO>Ar₂C═O>RCHO>R₂C═O>H₂C═0
Correct answer is option 'B'. Can you explain this answer?
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In nucleophilic substitution reactions, the reactivity of carbonyl com...
R < rcoor'="" />< rcho="" />< rcocl="" />< />
b) RCOCl < rcooh="" />< rcho="" />< rcoor'="" />< />
c) RCOOH < rcocl="" />< rcho="" />< rcoor'="" />< />
d) R < rcho="" />< rcoor'="" />< rcooh="" />< />
The correct answer is (b) RCOCl < rcooh="" />< rcho="" />< rcoor'="" />< r.="" this="" is="" because="" the="" reactivity="" of="" carbonyl="" compounds="" in="" nucleophilic="" substitution="" reactions="" is="" determined="" by="" the="" electron-withdrawing="" ability="" of="" the="" substituent.="" chlorine="" is="" a="" strong="" electron-withdrawing="" group,="" making="" rcocl="" the="" least="" reactive.="" carboxylic="" acids="" (rcooh)="" are="" also="" electron-withdrawing,="" but="" less="" so="" than="" chlorides,="" making="" them="" more="" reactive.="" aldehydes="" (rcho)="" and="" esters="" (rcoor')="" are="" less="" electron-withdrawing="" than="" carboxylic="" acids,="" making="" them="" more="" reactive.="" finally,="" ketones="" (r)="" do="" not="" have="" any="" electron-withdrawing="" groups,="" making="" them="" the="" most="" reactive.="" r.="" this="" is="" because="" the="" reactivity="" of="" carbonyl="" compounds="" in="" nucleophilic="" substitution="" reactions="" is="" determined="" by="" the="" electron-withdrawing="" ability="" of="" the="" substituent.="" chlorine="" is="" a="" strong="" electron-withdrawing="" group,="" making="" rcocl="" the="" least="" reactive.="" carboxylic="" acids="" (rcooh)="" are="" also="" electron-withdrawing,="" but="" less="" so="" than="" chlorides,="" making="" them="" more="" reactive.="" aldehydes="" (rcho)="" and="" esters="" (rcoor')="" are="" less="" electron-withdrawing="" than="" carboxylic="" acids,="" making="" them="" more="" reactive.="" finally,="" ketones="" (r)="" do="" not="" have="" any="" electron-withdrawing="" groups,="" making="" them="" the="" most="" />
b) RCOCl < rcooh="" />< rcho="" />< rcoor'="" />< />
c) RCOOH < rcocl="" />< rcho="" />< rcoor'="" />< />
d) R < rcho="" />< rcoor'="" />< rcooh="" />< />
The correct answer is (b) RCOCl < rcooh="" />< rcho="" />< rcoor'="" />< r.="" this="" is="" because="" the="" reactivity="" of="" carbonyl="" compounds="" in="" nucleophilic="" substitution="" reactions="" is="" determined="" by="" the="" electron-withdrawing="" ability="" of="" the="" substituent.="" chlorine="" is="" a="" strong="" electron-withdrawing="" group,="" making="" rcocl="" the="" least="" reactive.="" carboxylic="" acids="" (rcooh)="" are="" also="" electron-withdrawing,="" but="" less="" so="" than="" chlorides,="" making="" them="" more="" reactive.="" aldehydes="" (rcho)="" and="" esters="" (rcoor')="" are="" less="" electron-withdrawing="" than="" carboxylic="" acids,="" making="" them="" more="" reactive.="" finally,="" ketones="" (r)="" do="" not="" have="" any="" electron-withdrawing="" groups,="" making="" them="" the="" most="" reactive.="" r.="" this="" is="" because="" the="" reactivity="" of="" carbonyl="" compounds="" in="" nucleophilic="" substitution="" reactions="" is="" determined="" by="" the="" electron-withdrawing="" ability="" of="" the="" substituent.="" chlorine="" is="" a="" strong="" electron-withdrawing="" group,="" making="" rcocl="" the="" least="" reactive.="" carboxylic="" acids="" (rcooh)="" are="" also="" electron-withdrawing,="" but="" less="" so="" than="" chlorides,="" making="" them="" more="" reactive.="" aldehydes="" (rcho)="" and="" esters="" (rcoor')="" are="" less="" electron-withdrawing="" than="" carboxylic="" acids,="" making="" them="" more="" reactive.="" finally,="" ketones="" (r)="" do="" not="" have="" any="" electron-withdrawing="" groups,="" making="" them="" the="" most="" />
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In nucleophilic substitution reactions, the reactivity of carbonyl compounds follows the ordera)HCO>RCO>ArCO>RCHO>ArCHOb)HCO>RCHO>ArCHO>RCO>ArC0c)ArCO>RCO>ArCHO>RCHO>HCOd)ArCHO>ArCO>RCHO>RCO>HC0Correct answer is option 'B'. Can you explain this answer?
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In nucleophilic substitution reactions, the reactivity of carbonyl compounds follows the ordera)HCO>RCO>ArCO>RCHO>ArCHOb)HCO>RCHO>ArCHO>RCO>ArC0c)ArCO>RCO>ArCHO>RCHO>HCOd)ArCHO>ArCO>RCHO>RCO>HC0Correct answer is option 'B'. Can you explain this answer? for JEE 2024 is part of JEE preparation. The Question and answers have been prepared according to the JEE exam syllabus. Information about In nucleophilic substitution reactions, the reactivity of carbonyl compounds follows the ordera)HCO>RCO>ArCO>RCHO>ArCHOb)HCO>RCHO>ArCHO>RCO>ArC0c)ArCO>RCO>ArCHO>RCHO>HCOd)ArCHO>ArCO>RCHO>RCO>HC0Correct answer is option 'B'. Can you explain this answer? covers all topics & solutions for JEE 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for In nucleophilic substitution reactions, the reactivity of carbonyl compounds follows the ordera)HCO>RCO>ArCO>RCHO>ArCHOb)HCO>RCHO>ArCHO>RCO>ArC0c)ArCO>RCO>ArCHO>RCHO>HCOd)ArCHO>ArCO>RCHO>RCO>HC0Correct answer is option 'B'. Can you explain this answer?.
In nucleophilic substitution reactions, the reactivity of carbonyl compounds follows the ordera)HCO>RCO>ArCO>RCHO>ArCHOb)HCO>RCHO>ArCHO>RCO>ArC0c)ArCO>RCO>ArCHO>RCHO>HCOd)ArCHO>ArCO>RCHO>RCO>HC0Correct answer is option 'B'. Can you explain this answer? for JEE 2024 is part of JEE preparation. The Question and answers have been prepared according to the JEE exam syllabus. Information about In nucleophilic substitution reactions, the reactivity of carbonyl compounds follows the ordera)HCO>RCO>ArCO>RCHO>ArCHOb)HCO>RCHO>ArCHO>RCO>ArC0c)ArCO>RCO>ArCHO>RCHO>HCOd)ArCHO>ArCO>RCHO>RCO>HC0Correct answer is option 'B'. Can you explain this answer? covers all topics & solutions for JEE 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for In nucleophilic substitution reactions, the reactivity of carbonyl compounds follows the ordera)HCO>RCO>ArCO>RCHO>ArCHOb)HCO>RCHO>ArCHO>RCO>ArC0c)ArCO>RCO>ArCHO>RCHO>HCOd)ArCHO>ArCO>RCHO>RCO>HC0Correct answer is option 'B'. Can you explain this answer?.
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In nucleophilic substitution reactions, the reactivity of carbonyl compounds follows the ordera)HCO>RCO>ArCO>RCHO>ArCHOb)HCO>RCHO>ArCHO>RCO>ArC0c)ArCO>RCO>ArCHO>RCHO>HCOd)ArCHO>ArCO>RCHO>RCO>HC0Correct answer is option 'B'. Can you explain this answer?, a detailed solution for In nucleophilic substitution reactions, the reactivity of carbonyl compounds follows the ordera)HCO>RCO>ArCO>RCHO>ArCHOb)HCO>RCHO>ArCHO>RCO>ArC0c)ArCO>RCO>ArCHO>RCHO>HCOd)ArCHO>ArCO>RCHO>RCO>HC0Correct answer is option 'B'. Can you explain this answer? has been provided alongside types of In nucleophilic substitution reactions, the reactivity of carbonyl compounds follows the ordera)HCO>RCO>ArCO>RCHO>ArCHOb)HCO>RCHO>ArCHO>RCO>ArC0c)ArCO>RCO>ArCHO>RCHO>HCOd)ArCHO>ArCO>RCHO>RCO>HC0Correct answer is option 'B'. Can you explain this answer? theory, EduRev gives you an
ample number of questions to practice In nucleophilic substitution reactions, the reactivity of carbonyl compounds follows the ordera)HCO>RCO>ArCO>RCHO>ArCHOb)HCO>RCHO>ArCHO>RCO>ArC0c)ArCO>RCO>ArCHO>RCHO>HCOd)ArCHO>ArCO>RCHO>RCO>HC0Correct answer is option 'B'. Can you explain this answer? tests, examples and also practice JEE tests.
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