Select the expected major product of the reaction sequence shown. 1) Brz 2) 3 6q. NaNH/NH 3) H₂O O 3-methylhexyne O 1-bromo-3-methylhexybe O 2-bromo-3-methylhexyne O 3-methyl-1-hexyne O 3-methyl-2-hexyne
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- Draw a stepwise mechanism for the attached reaction that illustrateshow two substitution products are formed. Explain why 1-bromohex-2-ene reacts rapidly with a weak nucleophile (CH3OH) under SN1 reactionconditions, even though it is a 1 ° alkyl halide.Draw the most stable form of the major product in the reaction. 1. NaOC₂H5 2 2. H3O+, C2H5OHDraw the structure of compound A. Be sure to include stereochemistry.
- Alkyl diazonium salts decompose to form carbocations, which go on to form products of substitution, elimination, and (sometimes) rearrangement. Keeping this in mind, draw a stepwise mechanism that forms all of the following products.9) What is the major product in the following reaction? H₂ C H₂ A CN -NH₂ NO₂ 1) LIAIH, diethyl ether 2) H₂O B D NH₂ -N₂ LIAIHDraw the product formed from cyclohex-2-enone in each of three reactions. Reaction 1 Reaction 2 Reaction 1 1. NaCN 1. (CH3)2CuLi Reaction 2 product product 2. H3O*, H20 2. CH3CH21 A 1. EtO,CCH,CO¿Et NaOEt, HOET 2. Hао", Н-0, д Reaction 3 Reaction 3 product
- Choose the best reagents to complete the reaction shown below.Draw a stepwise mechanism for the following reaction that illustrates how two substitution products are formed. Explain why 1-bromohex-2ene reacts rapidly with a weak nucleophile (CH3OH) under SN1 reaction conditions, even though it is a 1 ° alkyl halide.Draw the major organic product of the following reactions. CO₂CH3 1. NaOCH3 2. H3O+ .CO₂CH3