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Setler [38]
3 years ago
12

What is the term given to a solution that contains the maximum amount of dissolved solute?

Chemistry
1 answer:
Marta_Voda [28]3 years ago
6 0

Answer: A super saturated solution

Explanation:

A super saturated solution is one which contains more solute than the solvent can dissolve

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Describe the effect of subjecting hydrogen to pressure​
ExtremeBDS [4]

Answer:

When hydrogen is subjected to large enough pressure, it solidifies according to theory.

Explanation:

According to theory, when  hydrogen molecules are subjected to enormous degree of pressure the molecules will solidify.

What happens here is that the hydrogen–hydrogen bonds in the hydrogen molecule will break apart and the molecules collapses into hydrogen atoms.

Hence, when hydrogen is subjected to large enough pressure, it solidifies according to theory.

3 0
3 years ago
Which of the following, in the solid state, would be an example of a metallic crystal?
e-lub [12.9K]
Iron because it is formed by metal atoms.
7 0
2 years ago
4. True or False. The longer a wire the greater its resistance.<br> O<br> True<br> False
Rudiy27

Answer:

TRUE

Explanation:

The total length of the wires will affect the amount of resistance. The longer the wire, the more resistance that there will be.

8 0
3 years ago
Name each compound. Do not capitalize element names. An example can be seen
miskamm [114]

Answer:

a. H2O: dihydrogen monoxide

b. PCl5: Phosphorus pentachloride

c. SiF4: Silicon tetrafluoride

d. N20: dinitrogen oxide

3 0
3 years ago
The displacement of a bromine atom by an amine is a substituion reaction. Write out the mechanism of this reaction (2--&gt;3) Wh
weqwewe [10]

Answer:

An alkyl halide can undergo SN2 reaction with an amine

Explanation:

The displacement of a bromine atom by an an amine (step 2---> 3) in the reaction sequence is an example of an SN2 reaction in which the amine is the nucleophile.

The nitrogen atom of the amine which bears a lone pair of electrons functions as the nucleophile and attacks the electrophilic carbon atom of the alkyl halide displacing the bromide and creating a new Carbon-Nitrogen bond. An ammonium intermediate is immediately formed and the reaction is completed by the abstraction of a hydrogen by a base (such as excess amine present in the system).

This reaction is slower with t-BuNH2 because of steric hindrance and steric crowding in the transition state. SN2 reactions are faster with methylamine where the alkyl carbon is easily accessible.

The detailed mechanism of this reaction has been attached to this answer.

4 0
3 years ago
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