2) Draw the for the O + CH,NH, 0 Cl,OLCCII, (c) .NH. ? H,C NO, +...

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2) Draw the for the O + CH,NH, 0 Cl,OLCCII, (c) .NH. ? H,C NO, + O,N NHNH, 2,4 dinitrophanyl- hydrazine ?? 3) Why was base required to get the reaction to go forward? In other words, why will hydroxylamine HCI and benzophenone not react on their own? 4) Ifyou camed out your reaction with phenylcyclohexyl ketone, you would have gotten the product shown below: ?? Unlike your product, this product can tautomerize (rearrange a double bond) to give an enamine. Why cant your product also ? Draw the enamine form of the compound above.

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