Faster reaction (towards top) R-CH2-OH R₂CH-OH R3COH Slower reaction (towards bottom) L
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Reorder this reactivity chart. But I think there's no need to reorder.
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- нно н но T 1 I T C-N C HHO H HO H-NCC-OH H-N-C C-OH > H-N-C HC-CH3 CH2 CH2 HC-CH3 CH3 CH2 CH2 CH3 ČH3 CH3 Figure 3.12 bond between two during a reaction. The accompanying figure shows the formation of a(n)Modify the structure to show the MAJOR product that would be formed in the following reaction. HNO3, H2SO4As2Cl3 chemical name
- a) What type of polymer is being formed in Reaction #3? b) Name an enzyme that can catalyze Reaction #3. c) What is △Go of Reaction #3? Show your work & clearly label your answer.Draw a curved arrow mechanism for the reaction, adding steps as necessary. Be sure to include all electrons that are necessary to the mechanism and all nonzero formal charges. о :0- 0-н .0. + Add/Remove step Click and drag to start drawing a structure.Suggest to biochemistry
- What substitution product are you expecting from the reaction below? NaCl O O O OH CI xo OCH 3 xox This reaction is unlikely to do a substitution reaction. 00 €H HN-C-C-OH H-C-CH, CH2 CH3 The following short passage is about the compound with chemical structure shown above. Use the following word bank to fill in the blanks in the passage. NOTE that some options may be used more than once: functional, L-serine, nonpolar, two, carboxyl, ketone, optimally, hydroxyl, three polar, neutral, methyl, L-isoleucine, four, amino, carbonyl, L-threonine, acidic, one, aldehyde, hydroxide, amine, D-threonine, asymmetrical, optically, D-serine basic, D-isoleucine, 2-hydroxybutanoic acid, L-glutamic acid, five, ionisable active compound with a maximum number of chiral carbon(s) Its is an example of a(n) chemical structure also contains a maximum number of ionisable group(s) at physiological pH. While the presence of a(n) group gives the compound its partial acidic properties group makes this compound nonpolar, the presence of a(n)НО b) HO 1) Name each listed compound (a, b, c, d) below, 2) Arrange them in a right reaction order for corresponded conjugation, and 3) List all involved enzyme(s) in each step. OH НО- OH COOH o-t=o OH Н н OH HN H ОН H H OH HN Н OH c) НО d) HO HO HO OH COOH OH O₂PO OH XR