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Draw the products formed when β-D-galactose is treated with below reagent.
NaH + C6H5CH2Cl
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- The following structure is D-sorbose. Which reagent will oxidize D-sorbose? CH2OH C = 0 Н-С-ОН НО - С - Н Н-С-ОН CH2OH Benedict's reagent None of the above Sodium hydroxide Tollen's reagent Barfoed's reagentA mixture of dipeptides consisting of Lys-Gly, Thr-His, Ser-Leu, Glu-Gln was applied to column packed with cation-exchange resin at pH 6.0. Which of these dipeptides would be eluted from the column first? O Lys-Gly first O Thr-His first O Ser-Leu first O Glu-Gln first OA mixture of Thr-His and Ser-Leu firstDraw the products formed when -D-idose is treated with C6H5NHNH2 (excess), H+
- Show the complete condensation reaction to form maltose. Label allmolecules.Certain microorganisms with a modified citric acid cycle decarboxylate α-ketoglutarate to produce succinate semialdehyde:With the G, L, + and – reactions, please tell me whether you would expect there to be a band in the agarose gel or not.
- Which of the following conversions require more than one step? 1. Alanine Ⓡpyruvate 2. Aspartate Ⓡoxaloacetate 3. Glutamate Ⓡa-ketoglutarate 4. Phenylalanine Ⓡhydroxyphenylpyruvate 5. Proline® glutamate O1 and 4 O 1, 2, and 4 O 1, 3, and 5 O2, 4, and 5 04 and 5 घWhat are the negative effects of using Disulfiram ?Below is an extract which describes the mechanism of action of aldolase during the cleavage of fructose 1, 6-bisphosphate to produce dihydroxyacetone phosphate (DHAP) and glyceraldehyde 3-phosphate (GAP). Fill in the missing words to complete the extract. Listed here is the pool of words to select from: abstracts, acidic, amine, covalent, hydroxyl, lysine, nitrogen, Schiff base, tetrahedral, water. Ring opening of F1,6BP occurs to render a linear sugar bisphosphate molecule.A __________ residue attacks the carbonyl carbon of F1,6BP. As the carbonyl Oxygen gets a negative charge, a proton is abstracted from the active site _________ amino acid. A _________ intermediate is produced. The active site basic amino acid residue _________ a proton from the lysine. A carbon- __________ double bond forms, producing a protonated Schiff base. At the same time, a solvent proton combines with the released hydroxyl group from C2 to form ________ and leaves the active site. The second active site…