QUESTION 13 Use these findings to answer the question. Compound X is optically inactive and has the formulaC 16H 16Br 2. On treatment with strong base, X gives hydrocarbon Y, C 16H 14. Compound Y absorbs 2 equivalents of hydrogen when reduced over a palladium catalyst and reacts with ozone to give two fragments. One fragment Z, is an aldehyde with formula C 7H 6O. The other fragment is glyoxal, (CHO) 2. The structure of X is: Br Ph Ph Br Br Br Ph Type: MC

Organic Chemistry
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Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
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Chapter22: Reactions Of Benzene And Its Derivatives
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Question 13
Br
QUESTION 13
Use these findings to answer the question.
Compound X is optically inactive and has the formulaC 16H 16Br 2. On treatment with strong base, X gives hydrocarbon Y, C 16H 14. Compound
Y absorbs 2 equivalents of hydrogen when reduced over a palladium catalyst and reacts with ozone to give two fragments. One fragment Z, is an
aldehyde with formula C 7H 6O. The other fragment is glyoxal, (CHO) 2.
The structure of X is:
Br
Ph
Br
Br
Br
Br
Ph
Ph
Type: MC
QUESTION 14
Use these findings to answer the question.
Compound X is optically inactive and has the formulaC 16H 16Br 2. On treatment with strong base, X gives hydrocarbon Y, C 16H 14. Compound
Y absorbs 2 equivalents of hydrogen when reduced over a palladium catalyst and reacts with ozone to give two fragments. One fragment Z, is an
aldehyde with formula C 7H 60. The other fragment is glyoxal, (CHO) 2-
The structure of Y is:
Transcribed Image Text:Br QUESTION 13 Use these findings to answer the question. Compound X is optically inactive and has the formulaC 16H 16Br 2. On treatment with strong base, X gives hydrocarbon Y, C 16H 14. Compound Y absorbs 2 equivalents of hydrogen when reduced over a palladium catalyst and reacts with ozone to give two fragments. One fragment Z, is an aldehyde with formula C 7H 6O. The other fragment is glyoxal, (CHO) 2. The structure of X is: Br Ph Br Br Br Br Ph Ph Type: MC QUESTION 14 Use these findings to answer the question. Compound X is optically inactive and has the formulaC 16H 16Br 2. On treatment with strong base, X gives hydrocarbon Y, C 16H 14. Compound Y absorbs 2 equivalents of hydrogen when reduced over a palladium catalyst and reacts with ozone to give two fragments. One fragment Z, is an aldehyde with formula C 7H 60. The other fragment is glyoxal, (CHO) 2- The structure of Y is:
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