For the stereoisomers below, use the r/s configuration given in the compound name to finish drawing the structure by connecting the appropriate groups. be sure to specify the stereochemistry via wedge-and-dash bonds. if needed, you may restore a module to its orignal state by clicking on the module and then clicking on the red over-under arrows.

If a bottle of olive oil contains 1.4 kg of olive oil, what is the volume, in milliliters ( ml ), of the olive oil?

Which type of orbits are found in the principal energy level n = 2 a - s b - s, f c - s, d d - s, p e - s, p, d

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.