Draw a curved arrow mechanism of the following SN2' reaction.  Make sure you show the intermediate structure.

To preview the image Click Here Give a curved arrow-pushing mechanism for the following reaction and make sure to include all nonbonding electrons. CLEARLY Indicate the initiation and propagation steps. H-Br CH3OOCH3 :Br: K

3. The haloalkane below is heated in a solution of ethanol and undergoes SN1 and E1S a) Draw the first step of the mechanism of the reaction. b) Show all the more stable carbocations that could be formed from (a). c) Draw all the El products that can be formed from (b). d) Circle the most favorable product(s) and explain your reasoning. e) Name: the most favored product(s).(Note: for cyclic alkenes the carbons of the C-C must be numbered 1,2 and in the name there is no need to specify its position). Br

Synthesis using a multiple RXN. A desired alkene product is shown below. A starting material is given. Propose a synthesis (2-3 step) of the molecule, include necessary reagents and the complete arrow. pushing mechanism for each reaction involved in the synthesis. S starting material Final product