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- A chemist synthesized compound X as a racemic mixture. When the ketone group in X was enzymatically reduced to the corresponding alcohol, a 100% yield was obtained of the product shown below. Choose the statement that best describes this result. ОН enzyme C;H1 `OCH,CH; pH 4.0 C3H1 `OCH,CH3 ОН ÕH X (racemic) (100% yield) One enantiomer of compound X reacts quickly with the enzyme. The other enantiomer of compound X is unreactive, but rapidly equilibrates with the reactive enantiomer under the reaction conditions. Since compound X was racemic, it makes sense that only a single product was obtained. O The product is a meso compound, so either enantiomer of compound X gives the same product. One enantiomer of compound X reacts quickly with the enzyme, while the other enantiomer of compound X remains unchanged.4. What are the products from the following reaction? H3O+ کاST03Q3137 Give the major product(s) of the following reaction. fuming H2SO4 (1 mole) heat
- (a) + H₂O H₂SO4C10T05Q3420 Give the major organic product for the following reaction. H H H catalytic heat if There is no reaction under these conditions or the correct product is not listed here.C15T05Q2545 Give the major product(s) of the following reaction. CH3CH2CI CI AICI3, heat CI CI CI CI- CI- CI There is no reaction under these conditions or the correct product is not listed here.
- 6) Which is the organic product for the following reaction? (a) (b) (c) (d) сон COOH ОН ОН COOH COOH KMnO4 H2OOn treatment with Cl2/hν, a compound with the formula C9H12 yields only a single monochloride. What is a possible structure of the compound?Provide the IUPAC name of the product formed from the following reaction. If no reaction is expected, write NR Br Ag₂O NHẠCH