Chapter 11: Q37. (page 450)
Question: alkyne gives each compound as the only product after hydroboration–oxidation?
a.
b.
Short Answer
Answer
a.
b.
Chapter 11: Q37. (page 450)
Question: alkyne gives each compound as the only product after hydroboration–oxidation?
a.
b.
Answer
a.
b.
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Get started for freeQuestion: Explain why an optically active solution of methylbutyrophenone loses its optical activity when dilute acid is added to the solution.
Convert each compound to hex-1-yne,
a.b.
c.
What two enols are formed when pent-2-yne is treated with H2O, H2SO4 and , HgSO4? Draw the ketones formed from these enols after tautomerization.
Question: Synthesize each compound from acetylene. You may see any other organic or inorganic reagents.
a.
b.
c.
d.
e.
Question: Devise a synthesis of each compound using CH3CH2CH=CH2as the starting material. You may use any other compounds or inorganic reagents.
a.
b.
c.
d.
e.
(+ enantiomer)
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