Answer:
NH3 has greater water solubility due to intermoleculate interactions
Explanation:
Hi:
If we represent the structures of NH3 and SbH3 we can see that they are similar to the naked eye, this is because N and Sb belong to the same group of the periodic table (group 15).
However, the electronegativity of N is greater than that of Sb. The NH3 molecule is polar and can form an intermolecular interaction called hydrogen bridge with water.
Sb is less electronegative than N. The SBH3 molecule forms an intermolecular interaction with water called dipole-induced dipole.
The zone with positive charge density of the water molecule (hydrogens) is oriented towards the zone with positive charge density of SBH3 (the pair of electrons not shared)
Stronger intermolecular junctions allow greater solubility of NH3 molecules.
Successes in your homework
Rubidium is a alkali metal.
Answer:
I assume you mean as in elements
A metal "A metal is a material that, when freshly prepared, polished, or fractured, shows a lustrous appearance, and conducts electricity and heat relatively well. Metals are typically malleable or ductile." (wiki)
a non-metal "In chemistry, a nonmetal is a chemical element that mostly lacks the characteristics of a metal. Physically, a nonmetal tends to have a relatively low melting point, boiling point, and density. A nonmetal is typically brittle when solid and usually has poor thermal conductivity and electrical conductivity." (wiki)
Explanation:
The reaction described above is the formation of an acetal. The initial starting material has a central carbonyl and two terminal alcohol functional groups. In the presence of acid, the carbonyl will become protonated, making the carbon of the carbonyl susceptible to nucleophilic attack from one of the alcohols. The alcohol substitutes onto the carbon of the carbonyl to provide us with the intermediate shown.
The intermediate will continue to react in the presence of acid and the -OH that was once the carbonyl will become protonated, turning it into a good leaving group. The protonated alcohol leaves and is substituted by the other terminal alcohol to give the final acetal product. The end result of the overall reaction is the loss of water from the original molecule to give the spiroacetal shown in the image provided.