Beginning with cyclohexanone, outline a synthesis of 2-benzylcyclohexanone. Display only covalent intermediates.
Synthesis: Outline a synthesis
of E from F.
Synthesis: Outline a synthesis of C from compound D.
Synthesis: Compound B from 3-chloro-2-methylbenzaldehyde
Compound B
Synthesis: Outline a synthesis of A from styrene and
ethanol.
A
19) Synthesis: Outline a synthesis of C from compound D. 20) Synthesis: Compound B from 3-chloro-2-methylbenzaldehyde CH Compound B 21) Synthesis: Outline a synthesis of A from styrene and ethanol. 18) Synthesis: Outline a synthesis of E from F.
using basic reactions and
grignard.
Outline a synthesis of the following compound from the compounds below as the only source of carbon incorporated into the final product, and any needed inorganic reagents. 2 OH , CH3 CH3 from 2 OH CH CH3
Outline a synthesis of the following compound from the compounds below as the only source of carbon incorporated into the final product, and any needed inorganic reagents. 2 OH , CH3 CH3 from 2 OH CH CH3
6. Using either malonic ester synthesis or acetoacetic ester synthesis, outline a reaction scheme in each case to show how you will synthesize compounds A and B below. [Show all steps with structure of all intermediates and necessary reagents). A. 3-butyl-2-tetradecanone B. 2-propylpentadecanoic acid
day/ date: to Outline the synthesis 2-methylpyrrolidine. Only the source of carbon. from propane use prop ane HN
4. Draw a reaction scheme for the synthesis of the oxime of cyclohexanone. age 2 of 2 95 WordsEnglish (US) 20 MacBook
Outline a synthesis of the following compound from the compound below as the only source of carbon incorporated into the final product, and any needed inorganic reagents. Ignore E/Z stereoisomers for the product alkene. from as the only source of carbon
Outline a synthesis of the following compound from the compound below as the only source of carbon incorporated into the final product, and any needed inorganic reagents. Ignore E/Z stereoisomers for the product alkene. from as the only source...
Starting with benzene or toluene, outline a synthesis of each of the following compounds using diazonium salts as intermediates a) 3,4,5-Tribromobenzonitrile b) 2,6-Dibromobenzoic acid
1) Using 3-methyl-1-butene as the only source of carbon, and any other reagents, outline a synthesis for each compound a) 3 b) c)
Propose reasonable synthesis for the following molecule in 2-5
steps. Show key intermediates but no mechanisms.Pr
Propose a reasonable synthesis for the following molecules 2999 1. HO3S
Put
the reagents and intermediates in correct order to complete the
following synthesis
Put the reagents and intermediates in correct order to complete the following synthesis. OH 1. MeMgør, Et20 2. H20 OH DMSO, C202Cl2 工 MgCl " | Mg, Et20 HgSO4, H2SO4, H20 H20