Answer:
A region on top of a mountain is cooler than at the base.
Explanation:
Pressure and temperature have direct relationship with each other. With the decrease in pressure, the temperature decreases and vice versa. When the air rises in the atmosphere, the pressure starts to fall. The low pressure at the peak of the mountains tends to cause the fall in temperature. It is because of this reason that it is cooler at the top of the mountain while the temperature is less cool in the foothills.
<span>The best answer is B. ICl experiences induced dipole-induced dipole interactions. Both iodine and chlorine belongs to the same group of the periodic table. Electronegativity decreases as you go down a group therefore Cl will have a greater attraction with the bond it forms with another atom. Dipole-dipole interactions form between I and Cl. For the Br2 molecule, no dipole occurs because they are two identical atoms. Therefore we will be expecting ICl will have a higher boiling point due to higher binding energy it forms.</span>
The correct option is (b)
NaNH2 is an effective base. It can be a good nucleophile in the few situations where its strong basicity does not have negative side effects. It is employed in elimination reactions as well as the deprotonation of weak acids.Alkynes, alcohols, and a variety of other functional groups with acidic protons, such as esters and ketones, will all be deprotonated by NaNH2, a powerful base.Alkynes are deprotonated with NaNH2 to produce what are known as "acetylide" ions. These ions are powerful nucleophiles that can react with alkyl halides to create carbon-carbon bonds and add to carbonyls in an addition reaction.Acid/base and nucleophilic substitution are the two types of reactions.Using the right base, terminal alkynes can be deprotonated to produce a carbanion.A good C is the acetylide carbanion.The acetylide carbanion can undergo nucleophilic substitution reactions because it is a potent C nucleophile. (often SN2) with 1 or 2 alkyl halides with electrophilic C to create an internal alkyne (Cl, Br, or I).Elimination is more likely to occur with 3-alkyl halides.It is possible to swap either one or both of the terminal H atoms in ethylene (acetylene) to create monosubstituted (R-C-C-H) and symmetrical (R = R') or unsymmetrical (R not equal to R') disubstituted alkynes (R-C-C-R').
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Both are oxidation reactions. Burning is just a lot faster than rusting.