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Consider the true/false of the following statements:
    S1: The most stable resonating structure of p-nitrophenol (not having aromatic ring) is .
    S2 : In  all C–O bonds are of equal length.
    S3 : CH3COONa is more resonance stabilised than the protonated acid CH3COOH.
    S4 : Benzene ring is more electron dense in phenol than phenoxide.
  • a)
    TTTT
  • b)
    FTTT
  • c)
    FTTF
  • d)
    FFTF
Correct answer is option 'C'. Can you explain this answer?
Verified Answer
Consider the true/false of the following statements: S1: The most stab...
S1: Most stable resonating structure is 
S4 : In  group has greater +m effect, so it makes phenoxide ion more electron dense.
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Most Upvoted Answer
Consider the true/false of the following statements: S1: The most stab...
S1: Most stable resonating structure is 
S4 : In  group has greater +m effect, so it makes phenoxide ion more electron dense.
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Consider the true/false of the following statements: S1: The most stable resonating structure of p-nitrophenol (not having aromatic ring) is . S2 : In all C–O bonds are of equal length. S3 : CH3COONa is more resonance stabilised than the protonated acid CH3COOH. S4 : Benzene ring is more electron dense in phenol than phenoxide.a)TTTTb)FTTTc)FTTFd)FFTFCorrect answer is option 'C'. Can you explain this answer?
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Consider the true/false of the following statements: S1: The most stable resonating structure of p-nitrophenol (not having aromatic ring) is . S2 : In all C–O bonds are of equal length. S3 : CH3COONa is more resonance stabilised than the protonated acid CH3COOH. S4 : Benzene ring is more electron dense in phenol than phenoxide.a)TTTTb)FTTTc)FTTFd)FFTFCorrect answer is option 'C'. 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 Consider the true/false of the following statements: S1: The most stable resonating structure of p-nitrophenol (not having aromatic ring) is . S2 : In all C–O bonds are of equal length. S3 : CH3COONa is more resonance stabilised than the protonated acid CH3COOH. S4 : Benzene ring is more electron dense in phenol than phenoxide.a)TTTTb)FTTTc)FTTFd)FFTFCorrect answer is option 'C'. Can you explain this answer? covers all topics & solutions for JEE 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for Consider the true/false of the following statements: S1: The most stable resonating structure of p-nitrophenol (not having aromatic ring) is . S2 : In all C–O bonds are of equal length. S3 : CH3COONa is more resonance stabilised than the protonated acid CH3COOH. S4 : Benzene ring is more electron dense in phenol than phenoxide.a)TTTTb)FTTTc)FTTFd)FFTFCorrect answer is option 'C'. Can you explain this answer?.
Solutions for Consider the true/false of the following statements: S1: The most stable resonating structure of p-nitrophenol (not having aromatic ring) is . S2 : In all C–O bonds are of equal length. S3 : CH3COONa is more resonance stabilised than the protonated acid CH3COOH. S4 : Benzene ring is more electron dense in phenol than phenoxide.a)TTTTb)FTTTc)FTTFd)FFTFCorrect answer is option 'C'. Can you explain this answer? in English & in Hindi are available as part of our courses for JEE. Download more important topics, notes, lectures and mock test series for JEE Exam by signing up for free.
Here you can find the meaning of Consider the true/false of the following statements: S1: The most stable resonating structure of p-nitrophenol (not having aromatic ring) is . S2 : In all C–O bonds are of equal length. S3 : CH3COONa is more resonance stabilised than the protonated acid CH3COOH. S4 : Benzene ring is more electron dense in phenol than phenoxide.a)TTTTb)FTTTc)FTTFd)FFTFCorrect answer is option 'C'. Can you explain this answer? defined & explained in the simplest way possible. Besides giving the explanation of Consider the true/false of the following statements: S1: The most stable resonating structure of p-nitrophenol (not having aromatic ring) is . S2 : In all C–O bonds are of equal length. S3 : CH3COONa is more resonance stabilised than the protonated acid CH3COOH. S4 : Benzene ring is more electron dense in phenol than phenoxide.a)TTTTb)FTTTc)FTTFd)FFTFCorrect answer is option 'C'. Can you explain this answer?, a detailed solution for Consider the true/false of the following statements: S1: The most stable resonating structure of p-nitrophenol (not having aromatic ring) is . S2 : In all C–O bonds are of equal length. S3 : CH3COONa is more resonance stabilised than the protonated acid CH3COOH. S4 : Benzene ring is more electron dense in phenol than phenoxide.a)TTTTb)FTTTc)FTTFd)FFTFCorrect answer is option 'C'. Can you explain this answer? has been provided alongside types of Consider the true/false of the following statements: S1: The most stable resonating structure of p-nitrophenol (not having aromatic ring) is . S2 : In all C–O bonds are of equal length. S3 : CH3COONa is more resonance stabilised than the protonated acid CH3COOH. S4 : Benzene ring is more electron dense in phenol than phenoxide.a)TTTTb)FTTTc)FTTFd)FFTFCorrect answer is option 'C'. Can you explain this answer? theory, EduRev gives you an ample number of questions to practice Consider the true/false of the following statements: S1: The most stable resonating structure of p-nitrophenol (not having aromatic ring) is . S2 : In all C–O bonds are of equal length. S3 : CH3COONa is more resonance stabilised than the protonated acid CH3COOH. S4 : Benzene ring is more electron dense in phenol than phenoxide.a)TTTTb)FTTTc)FTTFd)FFTFCorrect answer is option 'C'. Can you explain this answer? tests, examples and also practice JEE tests.
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