from Write a re vinylcycl reagents and relevant intermediates. trosynthetic analysis of the compound cis-1-butenylcyclohexane ohexane...
1. Name this compound according to the IUPAC system, including stereochemistry (cis/trans, EIZ), if relevant. CIS-3- isopropyl Cyclopent-l-ene 3 2. Using the compound in #1 as the starting material for all these reactions, write in the products, including stereochemistry if relevant: HBr 1. Hg(OAC)2, H20 2. NaBH Br2 1. BH, 2. H2O2, OH Bra H2O Pd mcpba
Write reaction schemes (unbalanced equations showing all reagents and products) for a synthesis of a compound with a hydride (H1- ) ion.
8. For the compound below provide a stepwise retrosynthetic analysis and a separate forward synthesis showing reagents and solvents used. Make sure you justify the regio- selectivity. (10 pts) and any other reagents
Synthesis with 10 steps or less
Synthesis Problem Show all the steps required, including intermediates, for the synthesis of the following target compound, using any starting material with six (6) carbons or less, plus any other organic or inorganic reagents necessary. Determine the IUPAC systematic chemical name for your target compound. Try for io sieps or tesvs
Synthesis Problem Show all the steps required, including intermediates, for the synthesis of the following target compound, using any starting material with six...
7. For the compound below provide a stepwise retrosynthetic analysis and a separate forward synthesis showing reagents and solvents used. Make sure you justify the regio- selectivity. (12 pts.) and any reagents of 2 carbons or less.
Show how the following compound could be prepared from 1-butyne. You may use any necessary reagents. You must show all stable intermediates formed along the way and all necessary reagents used (20 points). multiple steps!
1. Starting with benzene and any necessary reagents, design an efficient synthesis of the following compound: 1. Provide a detailed curved-arrow mechanism to account for the transformation below and explain why the only products formed at high and low temperatures are the ones shown. (Show all resonance contributors for all intermediates): HCl, Clos Cocha осн
Show how the following compound could be prepared from 1-butyne. You may use any necessary reagents. You must show all stable intermediates formed along the way and all necessary reagents used (20 points). multiple steps! Br
propose a synthesis for pentanamine from hexanoic acid. show all reagents and intermediates
1. Name this compound according to the IUPAC system, including stereochemistry (cis/trans, EIZ), if relevant. Z. Using the compound in #1 as the starting material for all these reactions, write in the products, including stereochemistry if relevant: HBT 1. Hg(OAc)2, H20 2. NaBH Brz 1. BH, 2. H2O2, OH Br; H20 H₂ Pd mcpba