- Messages
- 382
- Reaction score
- 315
- Points
- 73
Thank a lot.. much appreciated3c) You'll have to draw a double hump diagram for this. It's essentially the same as the simpler energy diagram except we break the single hump into 2 to represent the intermediate steps. There should be two peaks and the first one should be higher than the second. If you recall free radical substitution mechanism you know the intermediate steps. The first hump represents the formation of methyl free radical and HCl and the second represents the chloromethane formation. The reason the second hump is lower is because the reaction can only proceed as long as the energy barrier for the following step is less then the preceding one. The activation energy is labeled for the first hump.
4c) Ok, the final product is a ketone. Ketones come from the oxidation of secondary alcohols, so the intermediate must be a secondary alcohol. As you start with an Alkene you have to introduce an -OH group into the molecule so you use steam with conc. H3PO4. The result is CH3CH2CH(OH)CH3.
(For solving synthetic routes it helps if you go backwards, try thinking of the source of the product)
Hope this helps!