Show the retrosynthesis and the synthesis of the following compounds: OH Target material Starting material

Q: There are two kinds of aldolases. Class I aldolases are found in animals and plants, whereas class…

A: Aldolases are often used to convert fructose 1,6-biphosphate into dihydroxyacetone phosphate and…

Q: amidase NH2 HO, NH + K dabvana cocuai unt fan onzim amidace

A:

Q: 6-methyl-2-heptanone retrosynthesis/ synthesis

A: We have to synthesized 6-methyl-2-heptanone. We also have to give the retro-synthesis of…

Q: name of the compound and retrosynthesis of the compound

A: We have been asked outline a retrosynthetic pathway of this compound The IUPAC name of this compound…

Q: 3. Propose an acetoacetic ester synthesis to make 5-ethyl-6-methyl-2-heptanone.

A: Acetoacetic ester or ethyl acetoacetate is an active methylene compound and thus help in various…

Q: Draw the structure of the products formed when Arabinose shown above undergoes the following…

A: According to Q&A guidelines of Bartleby, we are supposed to answer only the first 3 sub-parts of…

Q: Show the mechanism of the reaction between Fumaric acid and bromine and identify the sterochemistry…

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Q: Table 1. Melting Points (°C) of Aldol Condensation Products1 Aldehyde i 113 175 129-130 144 Ketone &…

A: This question is based on interpretation of data given in table. In the given table, melting point…

Q: draw the structure of the major organic product made from the reaction provided please provide…

A: Anti-addition takes place.

Q: Draw the missing organic structures in the following multistep synthesis. Ignore any inorganic…

A: In the given question the amino group of amino acid is getting protected with the help of (BOC)2O.…

Q: What acetylide anion and epoxide are needed to synthesize attachedcompound?

A: Given:

Q: Draw the missing organic structures in the following multistep synthesis. Show all structures at…

A: The given reaction scheme is shown below.We have to provide the missing structure.

Q: Retrosynthesis: Show the starting materials that would make the desired product with the given…

A: Amine reacts with carbonyl compounds by a nucleophilic addition reaction mechanism. The product…

Q: Arabitol is produced by the reduction of D‑arabinose. Modify the molecule to show the product of the…

A:

Q: O

A: Base deprotonates the most acidic proton of cyclodiketone compound and inducible carbanion acts as…

Q: Enamines can serve as enolate surrogates in reactions at the a-carbon. In the reaction sequence, the…

A: The given reaction can be explained as :

Q: FADH2 reduces alpha,beta-unsaturated thioesters to saturated thioesters. The reaction is thought to…

A: The given reaction is shown below, The given substrate reacts with FADH2 and form corresponding…

Q: Carboxypeptidase A has esterase activity as well as peptidase activity, so it can hydrolyze ester…

A:

Q: 5. Give the major product(s) of the following chemical reaction. H₂N CH3 CH3 Ph Ph

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Q: What is the likely problem with doing a diethyl ether/water extraction on the following reaction…

A: Diethyl ether is a typical aprotic solvent used in laboratories. It is a hard Lewis base that reacts…

Q: If the following molecule cyclized, which of the following statements would be true? H- HO- HO H-…

A: it is the structure of galactose. It is a monosacharide. cyclization results when C5-OH doing…

Q: Complete the box complete reaction

A:

Q: ट ग्व HOTHQT

A: Given some incomplete reactions. Draw the structure of intermediate compound in retrosynthetic…

Q: One of the key components in fatty acid synthesis is acetoacetyl‑ACP, which is formed from a Claisen…

A:

Q: Kolbe-Schmitt reaction

A: Kolbe-Schmitt reaction or Kolbe reaction: Phenol is converted in to salicylic acid…

Q: A میر سیر - B OH + H OH

A: Here we have to write the mechanism of the following given multistep reaction.

Q: Use the priority system to draw the structure of the following molecule:…

A: Given that :We have to draw the structure of the following molecule using the priority system…

Q: -NH2 Na CN HCL, H,0 CN COCH 2-amino - 3-phenyl propanitrik phenylalanine COOH 02 H20 Iodinase COOH…

A:

Q: O True O False

A: Given statement: Acetylsalicyclic acid can be satisfactorily prepared through the acid catalysed…

Q: Show how the Gabriel synthesis could be used to make S-3-methyloctan1-amine. Indicate the mechanism…

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Q: Complete the following synthesis problem. Remember that all carbons in the synthesis target must…

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: What is the maior fiolact when reotl wnth acetic anhydride and pyridine

A: NH2 group attacks at carbonyl carbon of acetic anhydride because it is more nucleophilic as compared…

Q: What will be the complete hydrolysis products of the given structure below? CH2–0– -C17H37…

A: The given molecule is a phosphatidylcholine and it is the source of chlorine in the body. It…

Q: CI H3C ELOH, NaCN Br H3C DMF ÇI Na H;C CH3 éter

A: There are two types of nucleophilic substitution reactions. Unimolecular and bimolecular.

Q: Draw the structures of all possible products formed from the following reaction. Specify the type of…

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Q: Show the mechanism relating to the preparation of esters via Sn2 reactions ?

A: Esters are prepared when alcohols are added to carboxylic acid which occurs by the elimination of…

Q: 4. Following is the mechanism proposed for the inactivation of monoamine oxidase by…

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Q: There are two kinds of aldolases. Class I aldolases are found in animals and plants, whereas class…

A: solution- Aldolases are often used to convert  glyceraldehyde 3-phosphate. After bringing about this…

Q: Propose a mechanism for the biosynthesis of a-pinene from farnesyl pyrophosphate.

A: SInce  farnesyl pyrophosphate is present and we're following a biosynthesis and since farnesyl…

Q: Draw the structure of the product, substrate, or condition.

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Q: Reaction of diethyl acetamidomalonate with sodium ethoxide to form enolate anion 1; The enolate…

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Q: B

A: Retro = BackwardsSynthesis = The process of combining simpler reactions to form a chemical…