Chemistry, 08.05.2021 01:50 JAYDENJONES0111
The double mixed aldol condensation of 1,3-diphenylacetone with benzil in the presence of base gives an interesting product called 2,3,4,5- (tetracycline). Write a mechanism for this reaction and draw a structure for the product. This dark purple compound is an excellent Diels-Alder diene. Write the structure of the product formed from the Diels-Alder reaction of this material with methyl propanoate.
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Chemistry, 22.06.2019 07:20, rex1578
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
Answers: 1
Chemistry, 22.06.2019 23:20, svaskeacevilles5477
In medium-sized stars such as the sun, nuclear fusion almost always means the fusing of nuclei to form , but larger stars can produce elements as heavy as
Answers: 2
The double mixed aldol condensation of 1,3-diphenylacetone with benzil in the presence of base gives...
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