20. X and Y are enantiomers with chemical formula C,H10- A racemic mixture of X and Y treated with excess H, and Pd/C was converted to a single compound Z (C,H,12) which did not show optical activity. Suggest structure for X, Y and Z.

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Chapter1: Chemical Foundations
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15. Draw a dash-wedge structure for (R,cis)-hept-3-en-5-yn-2-
ol
16. Enantiomers have
physical properties.
17. The device that is used for measuring the effect of optically
active compounds on plane-polarized light is called a
18. If a sample is said to contain a 98.0% enantiomeric excess
of the compound (+)-camphor, what would be the observed
specific rotation if the pure (+)-camphor was found to have
a rotation of 44.1?
19. An equimolar mixture of two enantiomers is called a
20. X and Y are enantiomers with chemical formula C,H10: A
racemic mixture of X and Y treated with excess H, and
Pd/C was converted to a single compound Z (C,H1,) which
did not show optical activity. Suggest structure for X, Y
and Z.
21. The drug Crixivan (an HIV protease inhibitor) depicted
below, has
stereogenic centers.
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Transcribed Image Text:Search .ll 9:39 AM < Вack Assignment #2.docx 15. Draw a dash-wedge structure for (R,cis)-hept-3-en-5-yn-2- ol 16. Enantiomers have physical properties. 17. The device that is used for measuring the effect of optically active compounds on plane-polarized light is called a 18. If a sample is said to contain a 98.0% enantiomeric excess of the compound (+)-camphor, what would be the observed specific rotation if the pure (+)-camphor was found to have a rotation of 44.1? 19. An equimolar mixture of two enantiomers is called a 20. X and Y are enantiomers with chemical formula C,H10: A racemic mixture of X and Y treated with excess H, and Pd/C was converted to a single compound Z (C,H1,) which did not show optical activity. Suggest structure for X, Y and Z. 21. The drug Crixivan (an HIV protease inhibitor) depicted below, has stereogenic centers. Dashboard Calendar Тo Do Notifications Inbox 00
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