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4 Question (6 points) a Seepage 1026 Many organic syntheses exploit the presence of a particular functional group that is not present in the final product. Consider the desired synthesis of 3.6 dimethyl-3-octanol from 5-methyl-2-heptanone shown below. Ketones typically react as at the C=O carbon atom. A new CC bond is formed during this reaction, requiring a carbon containing carbon atoms. Part 2 (1 point) Which of the following are suitable reagents in their current forms for this transformation? Choose one or more: CH3CH2Li CH3CH2Br KCN ethylene oxide HCC Identify the carbon atoms in the product that correspond to C1 and C2 of the 5 -methyl-2-heptanone starting material. This synthenis can be completed in three steps as outlined below. Identify Reagent A (which is an organic compound) and the reagents required for each step. Reagents ( 9 items) (Drag and drop into the eppropriate area below) Reagents (9 items) (Dray and drop into the apponoporiute area below)