A compound with molecular formula C13H28 exhibits a 1H NMR spectrum with two signals: a septet with an integration of 1 and a doublet with an integration of 6. Draw the structure of this compound.

Achemist wants to extract copper metal from copper chloride solution. the chemist places 0.50 grams of aluminum foil in a solution containing 0.75 grams of copper (ii) chloride. a single replacement reaction takes place. (ii) chloride. a single replacement reaction takes place. which statement explains the maximum amount of copper that the chemist can extract using this reaction? a) approximately 0.36 grams, because copper (ii) chloride acts as a limiting reactant b) approximately 1.8 grams, because copper (ii) chloride acts as a limiting reactant c) approximately 0.36 grams, because aluminum acts as a limiting reactant d) approximately 1.8 grams, because aluminum acts as a limiting reactant

Which of these conditions most likely produces an unstable isotope?

Effect of rotenone and antimycin a on electron transfer rotenone, a toxic natural product from plants, strongly inhibits nadh dehydrogenase of insect and fish mitochondria. antimycin a, a toxic antibiotic, strongly inhibits the oxidation of ubiquinol. (a) explain why rotenone ingestion is lethal to some insect and fish species. (b) explain why antimycin a is a poison. (c) given that rotenone and antimycin a are equally effective in blocking their respective sites in the electron-transfer chain, which would be a more potent poison? explain.