Question Description
A neutral organic compound A(C10H20O2) neither reduces Tollen’s reagent nor forms precipitate with 2, 4-dinitrophenyl hydrazine, but can be resolved into enantiomers. A on acid hydrolysis forms two compounds B and C, both are enantiomeric. C neither reduces Fehling’s solution nor forms iodoform with alkaline iodine solution. C on oxidation with CrO3/HCI /pyridineforms D which is still resolvable into enantiomers. D on further treatment with aqueous (C2H5O)3 Al solution gives back A.Q.The correct statement regarding the following reaction isa)Product is achiralb)Product is a racemic mixturec)Product is a pair of diastereomerd)No α-halogenation occur with DCorrect answer is option 'B'. 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 A neutral organic compound A(C10H20O2) neither reduces Tollen’s reagent nor forms precipitate with 2, 4-dinitrophenyl hydrazine, but can be resolved into enantiomers. A on acid hydrolysis forms two compounds B and C, both are enantiomeric. C neither reduces Fehling’s solution nor forms iodoform with alkaline iodine solution. C on oxidation with CrO3/HCI /pyridineforms D which is still resolvable into enantiomers. D on further treatment with aqueous (C2H5O)3 Al solution gives back A.Q.The correct statement regarding the following reaction isa)Product is achiralb)Product is a racemic mixturec)Product is a pair of diastereomerd)No α-halogenation occur with DCorrect answer is option 'B'. 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 A neutral organic compound A(C10H20O2) neither reduces Tollen’s reagent nor forms precipitate with 2, 4-dinitrophenyl hydrazine, but can be resolved into enantiomers. A on acid hydrolysis forms two compounds B and C, both are enantiomeric. C neither reduces Fehling’s solution nor forms iodoform with alkaline iodine solution. C on oxidation with CrO3/HCI /pyridineforms D which is still resolvable into enantiomers. D on further treatment with aqueous (C2H5O)3 Al solution gives back A.Q.The correct statement regarding the following reaction isa)Product is achiralb)Product is a racemic mixturec)Product is a pair of diastereomerd)No α-halogenation occur with DCorrect answer is option 'B'. Can you explain this answer?.

Solutions for A neutral organic compound A(C10H20O2) neither reduces Tollen’s reagent nor forms precipitate with 2, 4-dinitrophenyl hydrazine, but can be resolved into enantiomers. A on acid hydrolysis forms two compounds B and C, both are enantiomeric. C neither reduces Fehling’s solution nor forms iodoform with alkaline iodine solution. C on oxidation with CrO3/HCI /pyridineforms D which is still resolvable into enantiomers. D on further treatment with aqueous (C2H5O)3 Al solution gives back A.Q.The correct statement regarding the following reaction isa)Product is achiralb)Product is a racemic mixturec)Product is a pair of diastereomerd)No α-halogenation occur with DCorrect answer is option 'B'. 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 A neutral organic compound A(C10H20O2) neither reduces Tollen’s reagent nor forms precipitate with 2, 4-dinitrophenyl hydrazine, but can be resolved into enantiomers. A on acid hydrolysis forms two compounds B and C, both are enantiomeric. C neither reduces Fehling’s solution nor forms iodoform with alkaline iodine solution. C on oxidation with CrO3/HCI /pyridineforms D which is still resolvable into enantiomers. D on further treatment with aqueous (C2H5O)3 Al solution gives back A.Q.The correct statement regarding the following reaction isa)Product is achiralb)Product is a racemic mixturec)Product is a pair of diastereomerd)No α-halogenation occur with DCorrect answer is option 'B'. Can you explain this answer? defined & explained in the simplest way possible. Besides giving the explanation of A neutral organic compound A(C10H20O2) neither reduces Tollen’s reagent nor forms precipitate with 2, 4-dinitrophenyl hydrazine, but can be resolved into enantiomers. A on acid hydrolysis forms two compounds B and C, both are enantiomeric. C neither reduces Fehling’s solution nor forms iodoform with alkaline iodine solution. C on oxidation with CrO3/HCI /pyridineforms D which is still resolvable into enantiomers. D on further treatment with aqueous (C2H5O)3 Al solution gives back A.Q.The correct statement regarding the following reaction isa)Product is achiralb)Product is a racemic mixturec)Product is a pair of diastereomerd)No α-halogenation occur with DCorrect answer is option 'B'. Can you explain this answer?, a detailed solution for A neutral organic compound A(C10H20O2) neither reduces Tollen’s reagent nor forms precipitate with 2, 4-dinitrophenyl hydrazine, but can be resolved into enantiomers. A on acid hydrolysis forms two compounds B and C, both are enantiomeric. C neither reduces Fehling’s solution nor forms iodoform with alkaline iodine solution. C on oxidation with CrO3/HCI /pyridineforms D which is still resolvable into enantiomers. D on further treatment with aqueous (C2H5O)3 Al solution gives back A.Q.The correct statement regarding the following reaction isa)Product is achiralb)Product is a racemic mixturec)Product is a pair of diastereomerd)No α-halogenation occur with DCorrect answer is option 'B'. Can you explain this answer? has been provided alongside types of A neutral organic compound A(C10H20O2) neither reduces Tollen’s reagent nor forms precipitate with 2, 4-dinitrophenyl hydrazine, but can be resolved into enantiomers. A on acid hydrolysis forms two compounds B and C, both are enantiomeric. C neither reduces Fehling’s solution nor forms iodoform with alkaline iodine solution. C on oxidation with CrO3/HCI /pyridineforms D which is still resolvable into enantiomers. D on further treatment with aqueous (C2H5O)3 Al solution gives back A.Q.The correct statement regarding the following reaction isa)Product is achiralb)Product is a racemic mixturec)Product is a pair of diastereomerd)No α-halogenation occur with DCorrect answer is option 'B'. Can you explain this answer? theory, EduRev gives you an ample number of questions to practice A neutral organic compound A(C10H20O2) neither reduces Tollen’s reagent nor forms precipitate with 2, 4-dinitrophenyl hydrazine, but can be resolved into enantiomers. A on acid hydrolysis forms two compounds B and C, both are enantiomeric. C neither reduces Fehling’s solution nor forms iodoform with alkaline iodine solution. C on oxidation with CrO3/HCI /pyridineforms D which is still resolvable into enantiomers. D on further treatment with aqueous (C2H5O)3 Al solution gives back A.Q.The correct statement regarding the following reaction isa)Product is achiralb)Product is a racemic mixturec)Product is a pair of diastereomerd)No α-halogenation occur with DCorrect answer is option 'B'. Can you explain this answer? tests, examples and also practice Class 12 tests.