The alcohol below was synthesized via a Grignard reaction. There are TWO different combinations of the Grignard reagent and carbonyl that can be used to make the product. Think about TWO ways to make the product, listing the carbonyl and Grignard reagent in the designated boxes.

10. Consider the below reaction between the acetylide ion and methanol. Draw the conjugate acid that is formed as a product in this reaction.

Please explain it in simple terms for someone who’s confused

Draw the major product of this reaction. Ignore inorganic byproducts. I I I I I I 1. Hg(Cl)2, CH3OH 2. NaBH4, NaOH Select to Edit OH Please select a drawing or reagent from the question area

Specify both the alcohol starting material and the reagents you would use in each step in a synthesis of the compound shown. If the synthesis requires only two steps enter "none" for step 3. r Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol Reagents available a. LiAlH₁ f. PBr3 b. H₂SO4 c. HCI d. HBr i. CH3 MgBr; then H3O+ e. SOC1₂ j. CH3 CH₂ MgBr; then H3O+ g. CrO3, H₂ SO4, H₂O h. NaH k. CH3 CH₂ CH₂ MgBr; then H3O+ I. C6H5 MgBr (phenylmagnesium bromide); then H3O+ m. (CH3)2 CHMgBr: then H3O+t n. Dess-Martin periodinane (DMP) Write the number/letters of the alchol/reagents in the boxes below. Alcohol starting material Reagent for step 1 Reagent for step 2 Reagent for step 3

Draw the structure of the organic product of the following transformation. Br cat. ACOH NH2

Draw the major product to each of the following reactions.