Answer:
Metals are good conductors of heat and electricity, and are malleable (they can be hammered into sheets) and ductile (they can be drawn into wire). Most of the metals are solids at room temperature, with a characteristic silvery shine (except for mercury, which is a liquid). Nonmetals are (usually) poor conductors of heat and electricity, and are not malleable or ductile; many of the elemental nonmetals are gases at room temperature, while others are liquids and others are solids.
Explanation:
Gas and liquid both take the shape of their container. The difference is gas molecules equally fills the space. Is there any more information?
Answer:
d. it has a high boiling point
Explanation:
all ionic compounds with ionic bonds have high boiling points
This is a combination reaction. Look at the 2 elements on left and a compound on the right.
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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