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Q: Draw structures of three possible Phase I metabolites of the following molecule. Name the reactions…
A: Answer is explained below.
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- By taking into account electronegativity differences, draw the products formed by heterolysis of the carbon–heteroatom bond in each molecule. Classify the organic reactive intermediate as a carbocation or a carbanion.Help with the structure of 2-chloro-2-phenylacetic acidDraw the product of the following reaction. Click the "draw structure" button to launch the drawing utility. t H₂SO4 draw structure
- When the ammonium salt (CH3CH2CH2)3NHCl is treated with NaOH, the products are water, NaCl, and an organic product. Provide the product in an attached file.According to the proposed schemes, write the equations of reactions. Be sure to write down the formulas of substances. α-D-glucopyranose + CH3IGiven the reaction of the synthesis of ethyl acetate: CH3COCH3 + Br2 + H3O+ → CH3COCH2Br + HBr + H3O+ Which is the catalyst? H3O+ CH3COCH3 CH3COCH2Br Br2
- 1. Bromine test is a test used to determine the degree of unsaturation in fatty acids. A colorless solution indicates a positive result. Which of the following fatty acids will not give a colorless solution? oleic acid Linoleic acid Lauric acid Linolenic acid 2. The following can cause the breaking of hydrogen bond, except? addition of silver nitrate heating agitation addition of acetic acid none of the aboveCarbonic anhydrase, an enzyme that converts carbon dioxide and water to carbonic acid as shown below, functions in the blood at an optimum pH of 7.0-7.5. Which of the following will lower the rate of carbonic anhydrase- catalyzed reaction? CO2 + H2O Carbonic anhydrase H₂CO3 O increasing the concentration of carbon dioxide O running the reaction at 4 °C carrying out the reaction at pH 7.2 O adding more carbonic anhydraseWhich compound forms the higher concentration of hydrate at equilibrium, PhCOCHO or PhCH2CHO? Explain your reasoning.