WebExpert Answer. Identify the reagent that can convert acetophenone into each of the following compounds. The phenyl group is abbreviated as "Ph" below. Note: If one or more reagents are incorrectly placed, a single red X will appear on the top left. (b) ia PAPhXc prie (1) LDA (2) CH2=CHCHMBP iar in onda Cla, NaOH, H20 Cl2, AcOH, H20 CH3CH2CHO ... WebIf you add the LiAlH4 slowly to the aldehyde, the aldehyde is always in excess. The relatively small amount of LiAlH4 present at any one time will reduce the most active …
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WebStarting from bromobenzene and any other reagents with two carbons or fewer, propose a synthesis of the compound shown. Choose the correct reagents for step 1. Mg, Et2O. … WebSolution. In the presence of ultraviolet light (but without a catalyst present), hot benzene will also undergo an addition reaction with chlorine or bromine. The ring delocalisation is permanently broken and a chlorine or bromine atom adds on to each carbon atom. For example, if you bubble chlorine gas through hot benzene exposed to UV light ... eviction notice ky
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WebTranscribed image text: Question 10 Starting from bromobenzene and any other reagents with two carbons or fewer, propose a synthesis of the compound shown. Br Choose the … WebThe Grignard reaction (pronounced Grin-yard) involves an R-Mg-X, a carbon chain bound to a magnesium halide, typically used to form alcohols by attacking carbonyls such as in aldehydes or ketones. The Grignard reaction is my go-to for chain elongation in orgo 2 synthesis. Alkynes are my go-to for orgo 1 chain elongation. WebAs the FeBr4 approaches, the electron poor hydrogen atom will easily bind with one of the electron rich bromine atoms. This is energetically favorable as well: hydrogen has an … eviction notice letter va