A 3 State which part of a plant cell:
makes food by photosynthesis
b
releases energy from food
controls what goes in and out of the cell
d stores information about making proteins
contains cell sap
f protects the outside of the cell.
с
e

Chloroplast

Release of energy from food : ATP

Explanation:

Chloroplasts are the cell organelles which contains chlorophyll and helps to trap energy in the unit known as photons and helps to utilize for preparing food.

a..Chloroplast

b..The mitochondria(a cell organelle)

d..an organism's DNA

f...the plasma membrane

the answer is c most of the fortnite players usually buy v bucks to get the battle pass and other cosmetics but some players who are referred to as "no skins" don't   buy skins and are usually noobs.

read more on -

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.