1) 2iaibj
Initially i deprotonate acetylene proton, which then attack on a.
Further Deprotonation by I which then attack on b and further hydrolysis give desired product.
2) 1igj
Deprotonation by i of 1 which then attack on g and hydrolysis give product.
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Specify a synthetic scheme that would produce the compound shown above in the fewest steps possible....
Specify a synthetic scheme that would produce the compound shown above in the fewest steps possible. Use one of the starting materials shown together with any of the available reagents. Give the number of the starting material followed by the letters of the reagents in the order of their use, for example: be Starting Materials COCaH5 C2H3OCCH COC2H. C2H3OCCH CCH, Available Reagents h. a. CHal CH.Br i. NaOC2H5 b. CH CHI j. H3O heat Br NaOH, H20. then H3O heat...
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[Review Topics References 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 stepsenter one for step 3 Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4.2.propanol 5. cyclohexanol Reagents available 3. LAH b. H,SO, e.HCI d. HB SOCI PB CrO, H, SOHO . NAH LCH, MgBr, then H, O J.CH,CH, MgBr; then H.O' k.CH,CH, CH, MgBr; then H,0 1.C, HMgBr...
Specify the reagent you would use in each step of the following synthesis: step 1 step 2 step 2 Reagents Available a. LIAIHA f. PBr3 b. H2SO4 c. HCI d. HBO e. SOC2 k. CH3CH MgBr g. Dess-Martin periodinane (DMP) I. CH.MgBr (phenylmagnesium bromide) h. Nah m. (CH3)2CHMgBr 1. NaOH n. Croz J. CH3MgBr Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2 Submit Answer Retry Entire Group 9 more group...
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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 Cl CH3 Alcohol Starting Materials 1. methanol 2. ethanol 3.1-propanol 4. 2-propanol 5. cyclohexanol Reagents available a. LiAlH4 f. PBr k. CH3 CH2CH2 then H3O L CsHsMgBr (phenylmagnesium bromide); then H3o m. (CHs)2CHMgBr: then Hgo d. HBr i. CH, MgBr, then Ho .Dess-Martin periodinane (DMP) e....