This compound, (C10H12O3), shows strong, sharp absorption between 1700 and 1720 cm-1, and strong, broad absorption over the region 2500-3000 cm-1. Given this information and the following NMR data, please draw the structure of the compound in the box below. 1H-NMR: 2.49 ppm, t(2H); 2.80 ppm, t(2H); 3.72 ppm, s(3H); 6.78 ppm, d(2H); 7.11 ppm, d(2H); 12.4, s(1H) 13C-NMR: 173.89; 157.87; 132.62; 128.99; 113.55; 54.84; 35.75; 29.20

4. absorption has the highest risk of overdose due to increased potency. a. rectal b. oral c. transdermal d. intranasal

Part b: study of equilibrium on solubility: mg(oh)2(s) ⇌ mg2+(aq) + 2 oh–(aq) cloudy clear (pink) 7. a. b. 8. a. b. 9. 10. 11. 12. when adding concentrated hydrochloric acid, how did the appearance of the equilibrium mixture change? the change in appearance indicated a shift in the point of equilibrium. in which direction did the equilibrium shift? (l) left (r) right explain your answer to question 7a. you should indicate which ion was added to or removed from the equilibrium mixture. when adding edta, how did the appearance of the equilibrium mixture change? the change in appearance indicated a shift in the point of equilibrium. in which direction did the equilibrium shift? (l) left (r) right explain your answer to question 8a. you should indicate which ion was added to or removed from the equilibrium mixture. upon heating in which direction is the equilibrium shifting? upon cooling in which direction is the equilibrium shifting? is the forward reaction a. endothermic explain your answers to questions 9, 10, and 11. (l) left (r) right (l) left (r) right b. exothermic

Which part of earth’s surface receives the most direct rays from the sun? a) equator b) ocean c) poles d) mountains