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- Give the expected organic product when phenylacetic acid, PhCH2COOH, is treated with reagent Q.)NaHCO3, H2OAspartame, the sweetener used in the commercial products NutraSweet and Equal, is 200 times sweeter than sucrose. What products will be obtained if aspartame is hydrolyzed completely in an aqueous solution of HCl?Aspartame, the sweetener used in the commercial products NutraSweet and Equal, is 200 times sweeter than sucrose. What products will be obtained ifaspartame is hydrolyzed completely in an aqueous solution of HCl?
- What product is formed when D-Gulose is treated with a. CH3I, Ag2O b. The product in (a), then H3O+ c. The product in (b), then C6H5CH2Cl, Ag2OPlease rank the following by increasing acidity: H2Se, H2O, CH4, H2SGive the expected organic product when phenylacetic acid, PhCH2COOH, is treated with reagent Q.)NaOH, H2O
- Compund ( A) C6H12 is treated with chlorine in the presence of carbon tetrachloride to given (B)C6H12Cl2.Compund (B) is treated with alcoholic KoH,followed by NaNH2 ,resulting in this formation of (C).compound (C) is treated with hydrogen in the presence of nickel catalysts to give 2methylpentane. Compound (C) does not react with sodamide or ammonical solution of silver nitrate .Ozonolysis of (A) give two aldehyde, (D) and (E) .Compound (E) is identified as acetaldehyde .From this information,describe the structural formula (A) ,(B) ,(C) And (C).write equation for all reactionIn an advanced synthetic chemistry experiment, a researcher prepares a compound, ZY-7, by reacting a ketone (C5H10O) with hydroxylamine (NH2OH), followed by heating in the presence of an acid catalyst. The resulting compound, ZY-7, is then treated with a solution of sodium nitrite (NaNO2) and hydrochloric acid (HCl) at low temperature. Identify the class of compound that ZY-7 most likely belongs to after this series of reactions." A) Amide B) Oxime C) Nitro compound D) Diazonium salt E) Ester Don't use chatgpt please provide valuable answerIdentify X in the following equation, and explain how hexanoic acid (Section 19.2B) is formed by this stepwise reaction sequence.
- From the given two compounds in the image, which reagents would differentiate the pair? a. Br2 in CH2Cl2 b. CrO3, H2SO4, acetone c. concentrated HCl with ZnCl2 d. aqueous FeCl3 e. aqueous NAHCO3 f. ammoniacal AgNo3An unknown hydrocarbon A with the formula C6H10 reacts with 1 molar equivalent of H2 over a palladium catalyst to give B C6H12 (Rxn 1). Hydrocarbon A also reacts with OsO4 to give the glycol C (Rxn 2). A gives 5-oxohexanal on ozonolysis (Rxn 3). Draw the structures of A, B, and C. Give the reactions.Treatment of -D-glucose with methanol in the presence of an acid catalyst converts it into a mixture of two compounds called methyl glucosides (Section 25.3A). In these representations, the six-membered rings are drawn as planar hexagons. (a) Propose a mechanism for this conversion and account for the fact that only the OH on carbon 1 is transformed into an OCH3 group. (b) Draw the more stable chair conformation for each product. (c) Which of the two products has the chair conformation of greater stability? Explain.