What are the main redox reactions in cellular respiration? glucose gains electrons through reduction while carbon dioxide loses those electrons through oxidation. glucose loses electron through oxidation while carbon dioxide gains those electrons through reduction. glucose loses electrons through oxidation while oxygen gains those electrons through reduction. glucose loses electrons through reduction while oxygen gains those electrons through oxidation.

At the time of aerobic respiration, the oxygen is taken up by the cells and in combination with glucose generates energy in the form of ATP, and the cell expels water and carbon dioxide. This is an oxidation-reduction reaction in which glucose is oxidized and oxygen is reduced.

In the entire process of oxidation, glucose is losing one or more electrons to oxygen, and in reduction, oxygen is gaining electrons.

Thus, the correct answer is glucose is losing those electrons through oxidation and oxygen gains those electrons through the process of reduction.

In cellular respiration, glucose loses electrons through oxidation while oxygen gains those electrons through reduction.

CELLULAR RESPIRATION:

C6H12O6+ 6O2 → 6CO2 + 6H2O

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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.