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Consider the reaction:
a. Write the equilibrium constant expression for this reaction.
If some hydrogen is added, before the reaction shifts:
b. How will the numerator and denominator of the expression in part a compare to the value at equilibrium?
c. Will
d. Will the reaction have to shift forward or backward to retain equilibrium? Explain.
e. Are your answers for b—d consistent with Le Chátelier’s principle? Explain.
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Chapter 15 Solutions
Solutions Manual For Chemistry: Structure And Properties
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- Problem 5-48 Assign R or S configurations to the chirality centers in ascorbic acid (vitamin C). OH H OH HO CH2OH Ascorbic acid O H Problem 5-49 Assign R or S stereochemistry to the chirality centers in the following Newman projections: H Cl H CH3 H3C. OH H3C (a) H H H3C (b) CH3 H Problem 5-52 Draw the meso form of each of the following molecules, and indicate the plane of symmetry in each: OH OH (a) CH3CHCH2CH2CHCH3 CH3 H3C. -OH (c) H3C CH3 (b) Problem 5-66 Assign R or S configurations to the chiral centers in cephalexin, trade-named Keflex, the most widely prescribed antibiotic in the United States. H2N H IHH S Cephalexin N. CH3 CO₂Harrow_forwardSteps and explanationn please.arrow_forwardSteps and explanationn please.arrow_forward
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