Match each synthesis of racemic leucine to what R has to be to complete it.  Answers may be repeated.

Q: Ph3P. Pd" Ph3P" transmetalation

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Q: Alanine has a methyl group as its sidechain on the alpha carbon. What property is associated with…

A: Amino acids are the biomolecules which are used in the synthesis of protein in human body. Amino…

Q: n some RNA molecules, a cytosine base is first methylated at N3 and then oxidatively deaminated in a…

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Q: Compound A Compound F HCI CH3OH H₂SO4 Compound B CH3 CH₂ CH₂ CI Compound E NaOH K₂Cr₂O7 H₂SO4…

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Q: 4. The polypeptide below is a target for prenylation. Draw the final processed polypeptide. QWAECAC

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Q: Choose the item in column 2 that best matches each item in column 1. Q26: Integrase A) Cell membrane…

A: We have been given five questions and we have been asked to identify given items.There are two types…

Q: Draw the mechanism for

A: Organic reactions can be defined as the reactions in which organic reactants react with each other…

Q: Match each synthesis of racemic leucine to what R has to be to complete it. Answers may be repeated.…

A: Synthesis of amino acid from carboxylic acid:

Q: Draw the organic products formed in the following reaction.

A: The first step is the reaction of given mixture of enantiomers of amino acid with acetic anhydride…

Q: What is the full name of this molecule? (β-D-Fructofuranose) And why is this molecule a reducing…

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Q: Please don't provide handwriting solution

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Q: NH2 tRNA но OH NN NH2 но OH N: „NH ATP tRNA "AMP-aa" N "ERNA-aa" O OH protein synthesis NEH. CO2 PPI…

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Q: Match each synthesis of racemic leucine to what R has to be to complete it. Answers may be repeated.…

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Q: 1. How would you synthesize adenosine monophosphate from ribose. Your synt path should be based on…

A: TRPM2 (transient receptor potential cation channel, subfamily M, member 2) is a nonselective cation…

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Q: Draw the mechanism for Fmoc deprotection. Hint: start with the most acidic proton on the Fmoc…

A: It is one of the efficient protection group for -NH2 functionality and can undergo deprotection in…

Q: what is the mechanism? How will galactose bind? NH2 Glactose Šugar EIOH/ACOH 'R

A: The detail solution is given below

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A: Any chiral center could have two possible configurations, and these configurations are designated…

Q: The following figure shows the intermediate of the transketolase mechanism. Use arrow pushing to…

A: Given reaction is : We need to draw the arrows depicting the mechanism and the final product.

Q: What is the product of the sequence shown? Br Br excess Mg D₂O Et₂O D D H H H3CO OCH3 ||| Mg Mg HO…

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Q: While there are proposals to explain the formation of sugars and nucleic aci bases separately, the…

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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: Define heterolytic cleavage.

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Q: Explain about N-formylmethionine (fMet) ?

A: N-formylmethionine, also known as fMet is a derivative of methionine amino acid. In this a formyl…

Q: The enzyme that catalyzes the C-Cg bond cleavage reaction that converts serine to glycine removes…

A: The chemical structure for PLP, serine, and glycine is shown below.

Q: 13.Draw the Fisher projection of the monosaccharide which gives the two diastereomeric aldoses upon…

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Q: For the chemical reaction shown on the left, please select all the statements that correctly…

A: Peptides: Two or more amino acids join together to form chains called peptides. In this the amino…

Q: 12. Classify each of the following compounds as reducing or non-reducing sugars: (3 Н НО OH OH OH OH…

A: I solved 3 questions...if you want more pls let me know..

Q: b the side chains of two molecules of isoleucine O ion-ion attraction O hydrogen bonding O disulfide…

A: The structure of isoleucine is shown below:

Q: NH2 H2N-DNA- H -N-DNA- H H2N-DNA- H2N OCH3 H2N. HN-DNA H3C NH H3C "NH2 Mitomycin C DNA adduct…

A: Reaction mechanism: A chemical reaction occurs by the sequence of elementary steps is called…

Q: RNAase, the enzyme that catalyzes the hydrolysis of RNA, has two catalytically active histidine…

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Q: Draw your own biosynthetic pathway showing the production of ALL the different types of glycosides.…

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Q: Draw the mechanism and product for each of the reactions in Problem 18.45 when they are catalyzed by…

A: (a) The mechanism of the first compound catalyzed by a base is given below :

Q: Draw an electron pushing mechanism for proline racemization. Draw a reaction coordinate diagram of…

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Q: Br

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Q: Draw the complete electron pushing mechanism that is enzyme catalyzed.

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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

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Q: N- Z-

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Q: Which of the compounds can undergo racemization at the alpha carbon?

A: Racemisation occurs one form of enantiomer is converted into equal proportion of other enantiomer…

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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.