Compound X is optically inactive and has the formula C 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. Which of the following answers is correct? The structure of Y is: The structure of Z is: Ph Br The structure of X is: Br The structure of Y is: Br The structure of X is: Ph Pn Br
Compound X is optically inactive and has the formula C 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. Which of the following answers is correct? The structure of Y is: The structure of Z is: Ph Br The structure of X is: Br The structure of Y is: Br The structure of X is: Ph Pn Br
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Compound X is optically inactive and has the formula C 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. Which of the following answers is correct? Select all that are correct.
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