OH II Hзо* Н но. O-P-O O-P-O glyceraldehyde 3-phosphate dihydroxyacetone phosphate O=d-'o

Q: H* + 1 mole equiv. CH3 HO-CH-CH3 H3C How would the product of the reaction be classified? O It is an…

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Q: Shown below is one of the reactions used in synthesizing Avanafil. What do we call this reaction? OH…

A: The reaction taking place is given as,

Q: Drawing an Enol and a Ketone Formed by Hydration of an Alkyne Draw the enol intermediate and the…

A: Enol intermediate and the ketone product formed in the reaction:

Q: CH;-0-C- methyl cyclopentancarboxylate O methyl cyclobutancarboxylate O ethyl cyclopentancarboxylate…

A: Using rules of IUPAC nomenclature we can name given compounds.

Q: The following isomerization reaction, drawn using D-glucose as starting material, occurs with all…

A: The stepwise formation of products is given below

Q: The following aldaric acid can lactonize to form two different products. Which ones? CO₂H НО -н H-OH…

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Q: B-D-Glucose, a hemiacetal, can be converted to a mixture of acetals on treatment with CH,OH in the…

A: Glucose exist in three form which are in equilibrium to each other. The first structure is fischer…

Q: During the metabolism of glucose, glyceraldehyde 3-phosphate is converted to dihydroxyacetone…

A: Keto –enol tautomerizations means the chemical equilibrium between enol form and keto form. Keto…

Q: What products are formed when each compound is treated with aqueous acid? OH OCH3 HỌ HOÇH2 NHCH,CH3…

A: When carbohydrates react with acid, then esterification takes place. Reaction of the hydroxyl groups…

Q: 1. CO2(s) 2. H,0, H2SO4 (3) MgX HO. Grignard reagent Carboxylic acid 1. R,CULI, THF 2. NH,CI, H2O HC…

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Q: Draw the organic product(s) of the following reaction. aqueous H,SO4 CH30 H. NaCN

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Q: Draw the one of the products formed when phenol (C,H5OH) is treated with the following reage [1]…

A: 1-Friedel craft alkylation  2-Benzylic bromination

Q: Draw the product of this reaction. Ignore inorganic byproducts. HO HO H H OH CH₂OH H₂ Pt Draw…

A: We have given reaction of carbohydrates with an H2,Pt. Which is reducing reagents.

Q: Determine the product formed when butanal (CH3CH2CH2CHO) is treated with each reagent. If no…

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Q: Draw a stepwise mechanism for the reaction of an alcohol with an isocyanate to form a urethane.

A: Here, nucleophilic attack occurs at the C of isocyanate by methanol to produce the urethane…

Q: What product is formed when each compound is treated with Tollens reagent (Ag 2O, NH 4OH)?

A: There are several tests available to identify the presence of certain functional groups in organic…

Q: Know the types of sugars that the following reagents react with and what physical appearances are…

A: Reducing sugars containing the aldehyde or ketone group in the carbohydrates that can act as the…

Q: Draw a stepwise mechanism for the following reaction, the last step in afive-step industrial…

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Q: Draw the product of this reaction. Ignore inorganic byproducts. H HO H OH H OH OH CH₂OH [H] Draw…

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Q: Complete the following Fischer esterification reaction

A: When an alcohol reacts with a carboxylic acid in the presence of an acid to form an ester is called…

Q: What product is formed when D-arabinose is treated with each reagent: (a) H 2 , Pd; (b) Benedict’s…

A: Arabinose contains a pentose ring with aldehyde group. It is also called as pectinose. It is found…

Q: 10. Which of the aldopentoses below will give an optically active aldaric ecid (di-ncid) on…

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Q: Draw the structure of the acyclic polyhydroxy aldehyde that cyclizes toattached hemiacetal.

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Q: Draw the product(s) of the following reactions. CH3CH₂CH₂-CEC-H 1. BH3/THF 2. H₂O₂ / aqueous NaOH

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Q: Comparing Hydration Products Using Two Different Methods Draw the product formed when CH3CH2C=CH is…

A: In hydroboration-oxidation reaction of alkene, a hydroxyl group is introduced to the carbon with…

Q: What products are formed when each compound is subjected to a Kiliani–Fischer synthesis?

A: The steps involved in Kiliani—Fischer synthesis of D-lyxose follows:Step-I Reaction of given aldose…

Q: Draw the product formed when pentanal (CH3CH2CH2CH2CHO) is treatedwith following reagent. With some…

A: Pentanal when treated with the given reagent (CH3MgBr, H2O) results in the formation of 2-hexanol

Q: During the metabolism of glucose, glyceraldehyde 3-phosphate is converted to dihydroxyacetone…

A: Keto –enol tautomerizations means the chemical equilibrium between enol form and keto form. Keto…

Q: draw structure for: o-Hydroxy-1,4 benzenedioicacid

A: In the chemical structure a hydroxy group is present and two carboxylic acids are present on benzene…

Q: Treatment of ethyl acetoacetate with NaOEt (2 equiv) and BrCH2CH2Br forms compound X. This reaction…

A: Sodium ethoxide (NaOEt) reagent mainly behaves as "nucleophile". It abstracts hydrogen that is…

Q: CH-CHCH-C—ОСН-CНСH3 + NaOH(ag) — CH3 CH3

A: Answer:- This question is answered by using the simple concept of hydrolysis of esters in basic and…

Q: What reagent is needed to convert 1-hexyne to 2-hexanone? O PCC (pyridinium chlorochromate) O BH3…

A: We have to tell which option is correct

Q: What product is formed when each compound is treated with either Ag2O, NH4OH or Na2Cr2O7, H2SO4,…

A: Since among the above reagents , Na2Cr2O7, H2SO4, H2O is a strong oxidising agent Hence they will…

Q: acetaldehyde dropwise NaOEt/EtOH NaOH, ETOH, H2O CI CI 1) NaOEt. EtOH (xs) Br(CH2)4Br OEt 2) NaOH,…

A: These are the examples of Aldol condensation and alkynation of active methylene compounds.

Q: .C. + CH,ОН CH;CH, CH2CH3

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Q: What products are formed when each ester is treated with H,O and H,SO,? b.tooi CH;CHCH, C.…

A: This is an example of acid catalysed hydrolysis of ester which result in the formation of carboxylic…

Q: Draw the structure of the product formed when 2-methylbutanal is treated with cold aqueous base.…

A: Please find below the reaction mechanism taking place.

Q: Treatment of ethyl acetoacetate with NaOEt (2 equiv) and BrCH2CH2Br forms compound X. This reaction…

A: The structure of "X" in the formation of illudin-S by acetoacetic ester synthesis is shown below.

Q: Sorbitol is a sweetener often used in chewing gum and diet drinks. It is obtained by the following…

A: The reagent used in the given reaction is H2.

Q: 6. Number of acyloin product(s) formed during this reaction. HOW Na Me-C-OEt + Et-C-OMe liq. NH3

A: Three acyloin products will form in the reaction

Q: Draw the product formed when phenylacetic acid (C6H5CH2COOH) istreated with following reagent. With…

A: Carboxylic acid is converted into amides on reaction with the amine in the presence of DCC. DCC acts…

Q: Draw the products formed when each acetal is treated with aqueous acid.

A: Since you have posted a question with multiple sub-parts, we will solve first three subparts for…

Q: how to find the thiol that can be oxidized to produce propyl disulfide,…

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Q: Draw the product formed when phenylacetic acid (C6H5CH2COOH) istreated with each reagent. With some…

A: Reaction of carboxylic acid with NaHCO3 liberates CO2.

Q: Draw the products formed when each ester is treated with lithium hydroxide and water. Reaction A…

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Reactions at the Alpha Carbon Atom

The position next to the ketone or aldehyde functional group is termed as alpha position and the reaction which occurs at alpha position is called alpha substitution reaction. In an alpha substitution reaction, the alpha proton atom is substituted by an electrophile by the formation of an enol intermediate or enolate ion intermediate. Most of the carbonyl compounds go through an alpha substitution reaction.