The reduced coenzymes generated by the citric acid cycle donate electrons in a series of reactions called the electron transport chain. the energy from the electron transport chain is used for oxidative phosphorylation.

which compounds donate electrons to the electron transport chain?
h 2 o o 2 adp fad fadh 2 nadh atp nad +
which compound is the final electron acceptor?
adp nadh h 2 o o 2 nad + fadh 2 atp fad
which compounds are the final products of the electron transport chain and oxidative phosphorylation?
fadh 2 adp fad o 2 h 2 o nadh nad + atp

The answer of ist question FADH2,NADH 2nd question O2  3rd question NAD+,FAD,H2O,ATP.

Explanation:

Ist answer

During electron transport chain electrons are donated by reduced coenzymes such as NADH and FADH2.

2nd answer

During electron transport chain oxygen or O2 act as terminal electron acceptor which accepts and then undergo reduction to generate H2O.

3rd answer

The final products of electron transport chain and oxidative phosphorylation are NAD+, FAD,H2O and ATP.

an individual’s sex (i.e., whether they are a male or female) is determined by the sex chromosomes. most people have two sex chromosomes, one that is inherited from their mother and one that is inherited from their father. typically, females have two x chromosomes (xx) and males have one x chromosome and one y chromosome (xy). conditions caused by changes (“mutations”) in genes located on the x chromosome are considered x-linked.

x-linked recessive inheritance

most x-linked conditions are recessive. this means that in a person with two x chromosomes (most females), both copies of a gene (i.e., one on each x chromosome) must have a change or mutation whereas in a person with one x chromosome (most males), only one copy of a gene must have a mutation. a female with a mutation in one copy of a gene on the x chromosome is said to be a “carrier” for an x-linked condition. a male with a mutation in a gene on the x chromosome is typically affected with the condition. because females have two copies of the x chromosome and males have only one x chromosome, x-linked recessive diseases are more common among males than females. however, x-linked recessive diseases can occur in both males and females.

for x-linked recessive disorders, an unaffected carrier mother who has a mutation in a gene on the x chromosome can transmit either the x chromosome with this mutation or a “normal” x chromosome to her children. if the father is unaffected, none of her daughters will be affected and all of her daughters will be unaffected—since they will inherit at least one normal x chromosome from their father. however, each daughter will have a 50% chance of being an unaffected carrier like her mother and a 50% chance of both x chromosomes being normal.