The purpose of photosynthesis is to Release chemical energy in the form of ATP for humans Release chemical energy in the form of ATP for humans Convert solar energy to chemical energy stored in sugar Convert solar energy to chemical energy stored in sugar Build proteins in plants

Convert solar energy to chemical energy stored in sugar

Explanation:

Photosynthesis is the process whereby green plants manufacture their food, which is in the form of a sugar (glucose). The photosynthetic process, generally, combines carbon dioxide (CO2) and water (H2O) in the presence of sunlight, which provides energy used.

The sugar (glucose) produced stores chemical energy in its chemical bonds. In a nutshell, photosynthesis converts SOLAR ENERGY (from sun) into CHEMICAL ENERGY (in glucose), which is the purpose of the process for organisms that undergo it.

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.

the answers are as following:

1. c. double helix, nucleosome, coil, supercoil, chromosome

2. b. g2 phase, preparation for mitosis

3. d. interphase consists of the g1, s, and g2 phases

4. c. metaphase

5. a. chromosomes are duplicated before cell division so that each new daughter cell has a complete set