Question 14 The hydrolysis of phosphoenolpyruvate proceeds with a AG" of about -62 kJ/mol. A major contributing factor to this reaction is the stabilization of the product pyruvate by: electrostatic attraction. O ionization. O polarization. resonance. tautomerization.
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Q: Molat Mass Review What is the Molar Mass of H₂SO4? What is the Molar Mass of Ca (OH)
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A: The answers are given below:
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A: Note : Since you have posted multiple questions, we are entitled to answer the first only. Please…
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A: pH of this solution can be calculated by considering acid, and salt composition.
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A: Option (C) and (H) are correct. Detail solution is given below:
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Q: 4. What are the products from the following reaction? H3O+ کا
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Q: ou!- complete the following reaction ? MaSH 9 <CO₂EE LIAIHA H NIH 200² (HN) ANTH thot
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Q: 10.0 g of NaHCO3 is dissolved in a mixture of 1750 mL water and 250 mL of 0.20 M NaOH. a. Calculate…
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Q: The activation energy of a reaction can be determined from the slope of which of the following…
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Q: Pd2+ + Cd2+ Cd (s) +Pd4+ E cell +0.323 V What is the potential of this cell reaction at 298 K when…
A: Given : [Pd2+] = 0.150M [Pd4+] =2 x 10-3M [Cd2+] = 0.200M E0cell = 0.323M
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- Please draw the product formed on protonation of ascorbic acid with HBr. Please explain the choice of site for protonation. Thank youOzonolysis, osmylation, and epoxide formation with mCPBA are all what type of reactions? a.) reduction b.)oxidation c) bothd) neither4) Draw and note the similarities of the cyanohydrin anion to Vitamin B1 ylide and BMIMCl ylide analyzing why pKa is in similar range 5) Analogously to the preparative stage of the citric acid cycle, pyruvic acid undergoes an oxidative decarboxylation to form acetaldehyde using the VitB1 ylide anion. Draw out this mechanism Please answer very soon will give rating surely Both questions answers needed
- Illustrate mechanisam for the hydrolysis of an acide chloride ?Draw the product of the reactions of succinic anhydride with each of the listed reagents. Assume in all cases that the reagent is present in excess and an aqueous workup takes place after each reaction. A. Reaction with (CH3)2CHOH. \table[[Select,Draw,Templates More,,],[/,//,I//,H,Erase]] B. Reaction with NH3. \table[[Select,Draw,tes More,Erase],[/,//,III,C,H,N,0]] Question Source: Vollhardt 7e0 Organic Chemistry: Structure And Function Publishęr: W. Freemar C. Reaction with phenylmagnesium bromide in THF, followed by H+,H2o. \table[[Select,Drav,v T,lates,,,Erase],[1,II,III,C,H,0,]] D. Reaction with LiAlH4 in ether, followed by H+,H2O \table[[Select,Draw,Templates More],[/,//,III]] \table[[3,0]] \table[[,2,QGiven the information pictured, The final step of the reaction sequence uses PhLi. Provide a reason and possible mechanism by which this final elimination and hydrolysis reaction would occur.
- Identify the lettered intermediates in the following reaction scheme. Thisis an alternative method to synthesize amino acids, based on the Gabrielsynthesis of 1° aminesWhich of the following represent the major intermediate in the acylation of anisole? Please explainThe given compound contains no alpha hydrogens.Will it undergo cannizarro reaction(including intramolecular)? Please explain.
- what pair of reagants can prepare diarylakene showna. What species other than an acid can be used to increase the rate of the transesterification reaction that converts methyl acetate to propyl acetate?b. Explain why the rate of aminolysis of an ester cannot be increased by H+, HO-, or RO-.how is the acetate synthesis isopentyl? show all steps please Arrows and all the movement of electrons