Compound J, C16H16Br2, is optically active. On treatment with strong base, compounds K and L (each C16H14) are formed; K and L each absorb only 2 equivalents of hydrogen when reduced over a Pd/C catalyst. Compound K reacts with ozone to give phenylacetic acid (C6H;CH,COOH), while similar treatment of L gives 2 products. One product, M, is an aldehyde with formula C-H,O; the other product is glyoxal (CHO),. Draw the structure of compound M. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Ignore alkene stereochemistry. • If more than one structure fits the description, draw them all. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate structures with + signs from the drop-down menu. C P ору aste ChemDoodle ramove

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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Compound J, C16H16B12, is optically active. On treatment with strong base, compounds K and L (each C16H14) are formed; K and L each absorb only
2 equivalents of hydrogen when reduced over a Pd/C catalyst. Compound K reacts with ozone to give phenylacetic acid (C,H,CH,COOH), while
similar treatment of L gives 2 products. One product, M, is an aldehyde with formula C-H,O; the other product is glyoxal (CHO),. Draw the structure
of compound M.
• Use the wedge/hash bond tools to indicate stereochemistry where it exists.
Ignore alkene stereochemistry.
• If more than one structure fits the description, draw them all.
• Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
Separate structures with + signs from the drop-down menu.
opy
aste
[F
ChemDoodle
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Transcribed Image Text:Compound J, C16H16B12, is optically active. On treatment with strong base, compounds K and L (each C16H14) are formed; K and L each absorb only 2 equivalents of hydrogen when reduced over a Pd/C catalyst. Compound K reacts with ozone to give phenylacetic acid (C,H,CH,COOH), while similar treatment of L gives 2 products. One product, M, is an aldehyde with formula C-H,O; the other product is glyoxal (CHO),. Draw the structure of compound M. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. Ignore alkene stereochemistry. • If more than one structure fits the description, draw them all. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate structures with + signs from the drop-down menu. opy aste [F ChemDoodle remove
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