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 X is: Br Ph Ph Br Br Br Br Br Ph Ph Туре: МC
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 X is: Br Ph Ph Br Br Br Br Br Ph Ph Туре: МC
Chapter14: Conjugated Compounds And Ultraviolet Spectroscopy
Section14.SE: Something Extra
Problem 50AP: -Ocimene is a pleasant-smelling hydrocarbon found in the leaves of certain herbs. It has the...
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Question
![Br
3-Bromo-4-chloro-2.5dimethythe xane
5-lodo-2-hexene
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
Br
Br
Br
Br
Ph
Ph
Турe: MC
QUESTION 14
Use these findings to answer the question.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F5bc418ab-5051-450d-ba5a-1e906e0fb9c9%2F233babcd-027f-449d-8641-a9a9cc24500a%2Fegxh49a_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Br
3-Bromo-4-chloro-2.5dimethythe xane
5-lodo-2-hexene
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
Br
Br
Br
Br
Ph
Ph
Турe: MC
QUESTION 14
Use these findings to answer the question.
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