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- Intermidiates and reagents of the following two final products from a Acetylene Note: the final products are different reactions but use the same starting material.Draw the alkene that would react with the reagent given to account for the product formed. ? + + H₂O **** H₂S04 • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. CH3 CH3 CHCCH3 | | OH CH3 +1Draw the alkene that would react with the reagent given to account for the product formed. ? + HCI My 3 You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. CH3 CH₂ CHOCH3 TT CI CH3 L ▼ {n [F ? ChemDoodleⓇ
- Which isomer of 1-bromo-3-isopropylcyclohexane reacts faster when refluxed with potassium tert-butoxide, the cis isomer or the trans isomer? Draw the structure of the expected product from the faster-reacting compound.4. Draw structural formulas for all possible monohalogenation products that might be formed in the following reactions, then assign them IUPAC names. (a) + Cl₂ light2. The following carbocation is generated as an intermediate in the addition of H-Br to an alkene. Draw the structure of all possible alkenes that could have formed this intermediate.
- Draw the expected major product when 1-octene reacts with Cl2 in aqueous solution (with H2O as the solvent).44a) Draw the bond-line structure of 1,4-dimethyl-cyclohexa-1,3-diene here: STRUCTURE: b) Circle all the sp²-hybridized carbons in your drawing of the structure. c) In the spaces below, draw two potential products from a chlorination reaction (addition of Cl2) with your first structure Product 1: Product 2:Which of these compounds would react with sodium methoxide to give onlỵ a single alkene product? .CI 1 4 O Compound 4 O Compound 3 O Compound 2 O Compound 1 O Compounds 3 and 4
- Draw a structural formula for the major organic product of the reaction shown below. H3C + (CH3)2CuLi ether You do not have to consider stereochemistry. #[ ] در ? H3O +Identify two alkenes that react with HBr to form 1-bromo-1-methylcyclohexane without undergoing a carbocation rearrangement.What alkene should be used to synthesize 3-bromohexane? 3-bromohexane