Protected amino group H2N. Z-CI OH HO, CH3 CH3 DCC Ala Bn (21-58) CH3 Bn-OH H,N, OH H2SO4 H2N. Bn Deprotection step H2 Pd Gly Protected carboxyl group H2N. OH Ala-Gly

Q: Provide a synthetic scheme along wi che reagents for the synthesis rglyceric acid from L-ascorbic…

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Q: Give the mechanism behind sodium azide inhibit peroxidase enzyme? If possible specific the…

A: inhibition of peroxidase enzyme by sodium azide.

Q: Which of the amines shown could, in principle, be used as a resolving agent for a racemic carboxylic…

A:

Q: Draw the structural formula for the a-D-glucosyl-(1-6)-D-mannosamine and circle the part of this…

A: Alpha-D-Glycosyl unit in which C-1 center are going to form glycosidic bond. D-mannosamine is a…

Q: (d) HO MOH Laurediol Br+ Bromoperoxidase Br ..OH Prelaureatin

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A: Pyranose and furanose are cyclic forms of sugar. Pyranose is six member sugar and  furanose is five…

Q: (d) Provide L-ascorbic acid from' D-glucose. the synthetic scheme for

A: Synthetic scheme for L-ascorbic acid from D-glucose is given below

Q: Predict the products from crossed Claisen condensation of the following pairs of esters. Indicate…

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Q: * Antimalarial (chloroquine) HN The molecule is acidic 2 Number of. is the location of chival chiral…

A: Given structure of chloroquine. determines its basicity and optical activity.

Q: How would you convert maleic acid 1 to tartaric acid 2 represented by meso-diastereomer? H. H HO…

A: We have find out the answer.

Q: Select all the molecules that are required for ring cleavage during the degradation of aromatic…

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Q: (d) Provide a curved arrow mechanism for the coupling of dipeptide to give tripeptide Boc-Ala-OH,…

A: Mechanism for the coupling reaction to make dipeptide in presence of HBTU and DIEA as coupling agent…

Q: ( H 6 chi nha + NH₂ → H₂ + H₂ Soy → Br- → complete the following reaction

A: #(i): NH2- is a strong base.  (CH3)2CH-O-H is a weak acid.

Q: How do you convert ethanamide to ethanamine, Name the reaction and Explain with Complete step by…

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Q: (1) 0 . Н le (ii) cởi Nha + NH2₂ + H₂ Soy - + Br- →

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Q: f) 3D structure of a natural dipeptide: Asp- Phe at neutral pl e) methyl B-D-gulopyranoside

A: Given: i. Structure of Methyl β-D-glucopyranoside ii. 3D structure of a natural dipeptides: Asp-Phe

Q: Consider the trisaccharide shown below. What is the designation of the glycosidic bond that connects…

A: The leftmost and middle monosaccharide glycosidic linkage is alpha(1 to 3) glycosidic linkage.…

Q: What are the major organic products of ozonolysis, followed by oxidative work-up, of each of the…

A: Oxidative Ozonolysis leads to formation of  carboxylic acid and ketones by cleavage of double bond .…

Q: Construct the Fischer, Haworth projection formulas and chair conformation (if applicable) of D-…

A: We have to draw the  Fischer, Haworth projection formulas and chair conformation of D-…

Q: In the figure below, His carries out generates| tetrahedral intermediate is stabilized by the by…

A: In the given figure, the lone pair of electron on the nitrogen of Histidine residue is donated to…

Q: Click the "draw structure" button to launch the drawing utility. Draw the furanose form of the…

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Q: None

A: Step-by-Step Instructions:Identify the Sequence:The sequence "NASTYPEAS" corresponds to:N:…

Q: Provide the name of a monosaccharide including its possible anomeric names. Provide the name for a…

A: The simplest unit of carbohydrates is known as monosaccharides. They cannot be broken down further…

Q: Outline, using chemical equations, the synthesis of the following from easily available…

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Q: Answer given full explanation..

A: Step-by-Step MechanismOxidation of Diphenhydramine:Enzyme Involvement: The process begins with the…

Q: Compound A is a D-aldopentose that can be oxidized to an optically inactive aldaric acid B. On…

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Q: What is the relationship between the compounds below? constitutional isomers identical compounds…

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Q: Give product me MCPBA

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: a) Give one possible binding interaction for the indicated group in the following compound in the…

A: In The given compound NH2 and COOH group both are present. So it remain as zwitter ion complex. So…

Q: Please provide degree of unsaturation for the following, and draw its structutre formula.

A: Given: C8H8O3 degree of unsaturation DOU = 2C+2+N-X-H2          here N = nitrogen atom = 0…

Q: Draw structure of product formed in cyanohydrin synthesis of ( S)- glyceraldehyde. Which products…

A: Cyanohydrins are addition products of HCN with carbonyl group. Glyceraldehyde is an  aldotriose with…

Q: HC CH3 HOOC COOH For this molecule, draw the structure of the pair of enantiomers.

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Q: Thoroughly explain why (a)malthose is a reducing sugar while trehalose is not based on their…

A: Monosaccharides are reducing sugars because they contain either an aldehyde group (if they are…

Q: R and Senantiomers. However, if only one were present, which isomers of hydrobenzoin are potential…

A: We have to choose the correct option.

Q: TⒸ Solved Synthesis of benzilic aciet from benzil bab, repart include discussion of result and…

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Q: photooxidative degradative process

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Q: НО CH,CH,CH,CH

A: Answer:IUPAC is the International Union of Pure and Applied Chemistry. It has given set of rules for…

Q: questions (a) -). CHO CHO CHO CHO CHO но но- HO H- OH H- OH HO H- H- OH HO- H- H- -ОН НО H- H- OH…

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Q: E. Starting with, alpha-ketoglutarate, ammonia and pyruvate, diagram, using structural formulae, the…

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Q: which is the most and least nucleophilicc, Arrange in the order of increasing nucleophlicity and…

A: The compounds given are,

Q: The stability of our genetic code depends on the stability of DNA. We are fortunate that the…

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Q: OCH3 H. H3C-X HX + deoxyribose a T residue of DNA deoxyribose O-4 alkylation product

A: Organic reaction mechanisms

Q: Compound A is a D-aldopentose that can be oxidized to an optically inactive aldaric acid B. On…

A: We have to answer the following questions

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.