FADH2's entrance point into the chain, complex II, is beyond the first "proton-pumping" site, complex I. Hence fewer ATP molecules are produced from FADH2 than from NADH.
Some of the energy released at each of the protein complexes I, III, and IV is consumed in the movement of H ions across the inner membrane from the matrix into the intermembrane space.
Movement of ions from a region of lower concentration (the matrix) to one of higher concentration (the intermembrane space) requires the expenditure of energy because it opposes the natural tendency, as exhibited in the process of osmosis (Section 8.9), to equalize concentrations.
Without oxygen as the final electron acceptor in the ETC, the ETC chain shuts down and ATP production stops. Without ATP to power life's processes (Chapters 24–26), these processes stop.
A protein in the mitochondria of brown fat cells that functions as an uncoupling agent, "uncoupling" the ATP production associated with the electron transport chain
Every acetyl CoA entering the citric acid cycle (CAC) produces three NADH, one FADH2, and one GTP (which is equivalent in energy to ATP; Section 23.6). Thus 10 molecules of ATP are produced for each acetyl CoA catabolized.
The conversion ATP -> ADP + Pi powers life processes (the biosynthesis of essential compounds, muscle contraction, nutrient transport, and so on). The conversion Pi + ADP -> ATP replenishes the ATP supply.