Asap in a do osmosis and diffusion have in common? a. both are the net movement of randomly moving molecules that makes concentration nearty equal on both sides of a bilayer membrane. b. both processes occur through a semipermeable membrane called a concentration gradient c. both require the additional energy provided by an energy-carrying molecule, like atp, to allow molecules to pass through the membrane. d. both permit molecules of any kind, whether solute or solvent, to cross the bilayer membrane.

The right answer is A.

Osmosis is a phenomenon that considers only the exchanges between two liquid solutions of different concentrations in liquid phases separated by a semi-permeable wall. Osmosis is a phenomenon of diffusion of matter, demonstrated when solvent molecules pass through a semi-permeable membrane separating two solutions whose solute concentrations are different; the overall transfer of solvent is then from the least concentrated solution (hypotonic medium) to the most concentrated solution (hypertonic medium) to equilibrium (isotonic media).

The diffusion of matter, or chemical diffusion, refers to the natural tendency of a system to render uniform the chemical potential of each of the chemical species it contains.

Chemical diffusion is an irreversible transport phenomenon that tends to homogenize the composition of the medium.

did you fail the test? xd

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.