The compounds which form hydrogen bonding should be determined from the given list. Concept Introduction: Intermolecular forces in a molecule are the important factor which is responsible for the physical changes of the molecule. The intermolecular forces in gases are negligibly small and the forces are comparatively stronger for liquids and the intermolecular forces are highest in solids. The stronger the intermolecular forces, closer will be the molecules in contact and thus higher will be the boiling point and melting point of the substance. Three types of intermolecular forces: London dispersion Dipole-dipole Hydrogen bonding Hydrogen bonding: It is an unusual strong intermolecular force occurs between a hydrogen atom and an electronegative atom like nitrogen, oxygen or fluorine. It occurs in both water and ammonia

Question

Want to see the full answer?

Answer 1

Question

Chapter 8.2, Problem 8.3P

Interpretation Introduction

Interpretation:

The compounds which form hydrogen bonding should be determined from the given list.

Concept Introduction:

Intermolecular forces in a molecule are the important factor which is responsible for the physical changes of the molecule.

The intermolecular forces in gases are negligibly small and the forces are comparatively stronger for liquids and the intermolecular forces are highest in solids.

The stronger the intermolecular forces, closer will be the molecules in contact and thus higher will be the boiling point and melting point of the substance.

Three types of intermolecular forces:

London dispersion

Dipole-dipole

Hydrogen bonding

Hydrogen bonding: It is an unusual strong intermolecular force occurs between a hydrogen atom and an electronegative atom like nitrogen, oxygen or fluorine.

It occurs in both water and ammonia

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

The beta-lactamase hydrolyzes the lactam-ring in penicillin. Describe the mechanism of hydrolysis, insuring to include the involvement of S, D, & K in the reaction sequence. Please help

To map the active site of beta-lactamase, the enzyme was hydrolyzed with trypsin to yield a hexapeptide (P1) with the following amino acids. Glu, Lys, Leu, Phe, Met, and Ser. Treatment of P1 with phenyl isothiocyanate yielded a PTH derivative of phenylalanine and a peptide (P2). Treatment of P1 with cyanogenbromide gave an acidic tetrapeptide (P3) and a dipeptide (P4).Treatment of P2 with 1-fluoro-2,4-dinitrobenzene, followed by complete hydrolysis, yields N-2,4-dinitrophenyl-Glu. P1, P2, and P3 contain the active site serine. Why doesn't D in this hexapeptide not participate in the hydrolysis of the beta-lactam ring even though S, K, and D are involved in the catalyst?

To map the active site of -lactamase, the enzyme was hydrolyzed with trypsin to yield a hexapeptide (P1) with the following amino acids. Glu, Lys, Leu, Phe, Met, and Ser. Treatment of P1 with phenyl isothiocyanate yielded a PTH derivative of phenylalanine and a peptide (P2). Treatment of P1 with cyanogenbromide gave an acidic tetrapeptide (P3) and a dipeptide (P4).Treatment of P2 with 1-fluoro-2,4-dinitrobenzene, followed by complete hydrolysis, yields N-2,4-dinitrophenyl-Glu. P1, P2, and P3 contain the active site serine. Using the experimental results described above derive the primary sequence of the active site hexapeptide. Please help!