HELP ILL MARK BRAINLIEST! 6. What is the chemical formula of glucose?
7. What is the chemical formula of fructose?
8. Do they contain hydroxyl groups?
9. Do they contain carboxyl groups?
10. What are these called?

6) C₆H₁₂O₆

7) C6H12O6

Fructose is recognized by having a five member ring and having six carbons, a hexose

Answer

6.C₆H₁₂O₆

7.C6H12O6

8.A hydroxyl group is a functional group that attaches to some molecules containing an oxygen and hydrogen atom, bonded together. Also spelled hydroxy, this functional group provides important functions to both alcohols and carboxylic acids. ... The oxygen is the red atom, while the hydrogen is represented by the grey atom

9.Carboxyl groups are commonly found in amino acids, fatty acids, and other biomolecules. An example of a less hydrophilic group is the carbonyl group (C=O), an uncharged but polar (contains partial positive and partial negative charges) functional group.

10. monosaccharides

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.