Acell goes through cellular respiration and produces atp which it then uses to move a molecule across the cell membrane. how does the energy in the original glucose molecule change during this process? a. the stored energy in the glucose is used to produce atp that can be converted to mechanical energy when the molecule moves across the cell membrane. b. the energy in the glucose is stored as kinetic energy in the atp and released as potential energy when the molecule moves across the cell membrane. c. the energy in the glucose is stored as mechanical energy in the atp and released as potential energy when the molecule moves across the cell membrane. d. the kinetic energy in the glucose is stored as potential energy in the atp and released as kinetic energy when the molecule moves across the cell membrane. -i think it's either a or d i just don't know about the type energy stored in glucose.

The correct answer is option D. The kinetic energy in glucose is stored as potential energy in ATP and released as kinetic energy when the molecule moves through the cell membrane.

Explanation:

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Let's solve this!

Oxygen (O2) is obtained through cellular respiration.

Oxygen breaks glucose molecules and generates ATP molecules.

The energy contained in the molecule is released and transformed into kinetic energy.

After this analysis, we conclude that the correct answer is option D. The kinetic energy in glucose is stored as potential energy in ATP and released as kinetic energy when the molecule moves through the cell membrane.

doctors i believe if i'm wrong sorry

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.