9which molecule can mix with water and is also a source of energy and a storage
area for energy in the body?
a lipid
b chlorophyll
c nucleic acid
d carbohyd

Lipid can mix with water and is also a source of energy and a storage  area for energy in the body

Explanation:

Lipid is most commonly called fats, which is mainly composed with hydrogen and oxygen. It has limited amount of nitrogen, oxygen, sulfur and phosphorus. It is source of nutrients. It serves as many ways and purposes. It plays vital role in structure and also function of organism.

It gives energy as well as thermal insulation. Some lipids work as chemical messenger between cells, tissue and organs. These lipids are steroid hormone.

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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.