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 (C6H5CH2COOH), while similar treatment of L gives 2 products. One product, M, is an aldehyde with formula C7H6O; the other product is glyoxal (CHO)2. Draw the structure of compound M. Use wedge and dash bonds to indicate stereochemistry.

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1. why does the same side of the moon always face earthc.the rotational period of the moon is equal to one revolution around earth2. which is greater the moons period of rotation or its period of revolution  b.the moons revolution period around earth3.what was the major accomplishment of the apollo missions  c.sending the first human into space4. which of these space missions involved the deployment of lunar roversa. voyager 15. which scientists are going to explore next on kepler-186fd. evidence of existence of life6.which mission is not going to explore the outside of the solar  systemb.safir7.which technology limit the future of space explorationb. scientist must first develop certain technologies before missions can be completed.

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