Please help me with the skeletal (line) structure of the following molecule:
Ethyl 2,6-diethyl-4,5,6-trihydroxy-3-oxooct-7-enoate
And this question has me stumped!...
An unknown compound W has the molecular formula C8H8 and so clearly has a large degree of unsaturation. However, when reacted with excess bromine the only product, compound X, has the molecular formula C8H8Br2. When more vigorous conditions are applied to compound X, including heat and a catalyst, two new compounds Y and Z are then formed each with the formula C8H7Br3.
Draw possible skeletal (line) structures that might represent the products W - Z.
--> ---->
C8H8 Br2 C8H8Br2 Br2 / catalyst (Heat) C8H7Br3
(W) (X) (Y and Z)
Thankyou, any help is appreciated.