Answer:
extensive hydrogen bonding
Explanation:
The high boiling points of water, hydrogen fluoride (HF) and ammonia (NH3) is an effect of the extensive hydrogen bonding between the molecules. The London dispersion force is caused by random and temporary changes in the polarity of atoms, caused by the location of the electrons in the atoms' orbitals.
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When two element combine to form more than one compound i hope this helps you with work have a nice day :)
Answer:
The value of dissociation constant of the monoprotic acid is
.
Explanation:
The pH of the solution = 2.46
![pH=-\log[H^+]](https://tex.z-dn.net/?f=pH%3D-%5Clog%5BH%5E%2B%5D)
![2.46=-\log[H^+]](https://tex.z-dn.net/?f=2.46%3D-%5Clog%5BH%5E%2B%5D)
![[H^+]=0.003467 M](https://tex.z-dn.net/?f=%5BH%5E%2B%5D%3D0.003467%20M)

Initially
0.0144 0 0
At equilibrium
(0.0144-x) x x
The expression if an dissociation constant is given by :
![K_a=\frac{[A^-][H^+]}{[HA]}](https://tex.z-dn.net/?f=K_a%3D%5Cfrac%7B%5BA%5E-%5D%5BH%5E%2B%5D%7D%7B%5BHA%5D%7D)

![x=[H^+]=0.003467 M](https://tex.z-dn.net/?f=x%3D%5BH%5E%2B%5D%3D0.003467%20M)


The value of dissociation constant of the monoprotic acid is
.
Answer:
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Answer:
Diasteriomers
Stereoisomers
Stereoisomers
Meso compounds
Constitutional isomers
Enantiomers
Enantiomers
Explanation:
Isomers are compounds that posses the same molecular formula but different structural formulas.
Constitutional isomers differ only in atom to atom connectivity while stereoisomers differ in arrangement of atoms in space. Stereo isomers differ in physical and chemical properties of the compounds.
When stereo isomers are non-superimpossible mirror images of each other, they are called enantiomers. Enantiomers have the same chemical and physical properties and differ only in their reaction with chiral substances.
Achiral compounds are compounds that do not exhibit chirality. Some achiral compounds contain stereogenic centers and are called meso compounds.