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Treatment of 2,4-pentanedione with excess of KCN(aq)and acetic acid followed by hydrolysis in thepresence of H2SO4 gives two products A and B, both having molecular formula C7H12O6. When heated, B first gives a lactonic acid C7N10O5 and finally a dilactone P (C7H8O4).Q.What is the correct structure of P?a)b)c)d)Correct answer is option 'C'. Can you explain this answer? for Class 12 2024 is part of Class 12 preparation. The Question and answers have been prepared
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the Class 12 exam syllabus. Information about Treatment of 2,4-pentanedione with excess of KCN(aq)and acetic acid followed by hydrolysis in thepresence of H2SO4 gives two products A and B, both having molecular formula C7H12O6. When heated, B first gives a lactonic acid C7N10O5 and finally a dilactone P (C7H8O4).Q.What is the correct structure of P?a)b)c)d)Correct answer is option 'C'. Can you explain this answer? covers all topics & solutions for Class 12 2024 Exam.
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Treatment of 2,4-pentanedione with excess of KCN(aq)and acetic acid followed by hydrolysis in thepresence of H2SO4 gives two products A and B, both having molecular formula C7H12O6. When heated, B first gives a lactonic acid C7N10O5 and finally a dilactone P (C7H8O4).Q.What is the correct structure of P?a)b)c)d)Correct answer is option 'C'. Can you explain this answer?, a detailed solution for Treatment of 2,4-pentanedione with excess of KCN(aq)and acetic acid followed by hydrolysis in thepresence of H2SO4 gives two products A and B, both having molecular formula C7H12O6. When heated, B first gives a lactonic acid C7N10O5 and finally a dilactone P (C7H8O4).Q.What is the correct structure of P?a)b)c)d)Correct answer is option 'C'. Can you explain this answer? has been provided alongside types of Treatment of 2,4-pentanedione with excess of KCN(aq)and acetic acid followed by hydrolysis in thepresence of H2SO4 gives two products A and B, both having molecular formula C7H12O6. When heated, B first gives a lactonic acid C7N10O5 and finally a dilactone P (C7H8O4).Q.What is the correct structure of P?a)b)c)d)Correct answer is option 'C'. Can you explain this answer? theory, EduRev gives you an
ample number of questions to practice Treatment of 2,4-pentanedione with excess of KCN(aq)and acetic acid followed by hydrolysis in thepresence of H2SO4 gives two products A and B, both having molecular formula C7H12O6. When heated, B first gives a lactonic acid C7N10O5 and finally a dilactone P (C7H8O4).Q.What is the correct structure of P?a)b)c)d)Correct answer is option 'C'. Can you explain this answer? tests, examples and also practice Class 12 tests.