The intermolecular forces that stabilize the structure of DNA and their action is to be determined. Concept introduction: The intermolecular forces are the forces that act between molecules, atoms or ions. They are relatively weak forces of attraction. The intermolecular forces are of five types as hydrogen bonding, ionic bonding, ion-dipole forces, ion-induced dipole forces, van der Waals forces. DNA or deoxyribonucleic acid is the hereditary material in humans and almost all living organisms. Most of it is present in the cell nucleus (nuclear DNA) and some are located in the mitochondria (mitochondrial DNA). DNA has four chemical bases as adenine (A), guanine (G), cytosine (C) and thymine (T). The sequence of these bases provides information that is used to build and maintain organisms.

Question

Want to see the full answer?

Answer 1

Question

Chapter 13, Problem 13.18P

Interpretation Introduction

Interpretation:

The intermolecular forces that stabilize the structure of DNA and their action is to be determined.

Concept introduction:

The intermolecular forces are the forces that act between molecules, atoms or ions. They are relatively weak forces of attraction.

The intermolecular forces are of five types as hydrogen bonding, ionic bonding, ion-dipole forces, ion-induced dipole forces, van der Waals forces.

DNA or deoxyribonucleic acid is the hereditary material in humans and almost all living organisms. Most of it is present in the cell nucleus (nuclear DNA) and some are located in the mitochondria (mitochondrial DNA). DNA has four chemical bases as adenine (A), guanine (G), cytosine (C) and thymine (T). The sequence of these bases provides information that is used to build and maintain organisms.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Using the graphs could you help me explain the answers. I assumed that both graphs are proportional to the inverse of time, I think. Could you please help me.

Synthesis of Dibenzalacetone [References] Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone below. Question 1 1 pt Question 2 1 pt Question 3 1 pt H Question 4 1 pt Question 5 1 pt Question 6 1 pt Question 7 1pt Question 8 1 pt Progress: 7/8 items Que Feb 24 at You do not have to consider stereochemistry. . Draw the enolate ion in its carbanion form. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. ⚫ Separate multiple reactants using the + sign from the drop-down menu. ? 4

Shown below is the mechanism presented for the formation of biasplatin in reference 1 from the Background and Experiment document. The amounts used of each reactant are shown. Either draw or describe a better alternative to this mechanism. (Note that the first step represents two steps combined and the proton loss is not even shown; fixing these is not the desired improvement.) (Hints: The first step is correct, the second step is not; and the amount of the anhydride is in large excess to serve a purpose.)