<u>Answer:</u>
For 2: The correct answer is grams of solute per 100 grams of solvent.
For 3: The correct answer is supersaturated.
For 4: the correct answer is the solubility decreases.
<u>Explanation:</u>
Solubility is defined as the property which refers to the ability of the solute that can be dissolved in a solvent. It is defined as the number of grams of solute per 100 grams of solvent.
Unsaturated solution is defined as the solution in which amount of solute that is dissolved in the solvent is less.
Saturated solution is defined as the solution in which no more solute can be dissolved in the given amount of solvent.
Emulsion is defined as the dispersion of one liquid in another liquid in which it is not soluble.
Supersaturated solution is defined as the solution in which solvent contains more amount of solute than the required amount. These solutions help in the process of crystallization.
When a crystal is added to a <u>supersaturated solution</u>, more and more particles come out of the solution and this process is known as crystallization.
According to the Henry's Law
The solubility of the gas in a liquid is directly proportional to the partial pressure of the gas.
With increase in the partial pressure, the solubility of the gas in liquid also increases and vice-versa.
Hence, the correct answer is the solubility decreases.
Answer:
To support and protect the cell.
Explanation:
The cell was (only found in plant cells) are there to help the plasma membrane and help the plant hold its structure. If the cell wall wasn't there the plant would just flop onto the ground!
-Good luck-
Answer:
1 mole of iron (Fe) = 56 g (molar mass)
Since 56 g of iron = 1 mol.
Therefore, 112 g of iron= 1/ 56 ×112 mol = 2 mol.
Explanation:
<h3><u>Full Question:</u></h3>
The following compound has been found effective in treating pain and inflammation (J. Med. Chem. 2007, 4222). Which sequence correctly ranks each carbonyl group in order of increasing reactivity toward nucleophilic addition?
A) 1 < 2 < 3
B) 2 < 3 < 1
C) 3 < 1 < 2
D) 1 < 3 < 2
<h3><u>Answer: </u></h3>
The rate of nucleophilic attack of carbonyl compounds is 2<3 <1.
Option B
<h3><u>Explanation. </u></h3>
Nucleophilic attack is explained as the attack of an electron rich radical to a carbonyl compound like aldehyde or a ketone. A nucleophile has a high electron density, so it searches for a electropositive atom where it can donate a portion of its electron density and become stable.
A carbonyl compound is a 
hybridized carbon atom with a double bonded oxygen atom in it. The oxygen atom pulls a huge portion of electron density from carbon being very electropositive.
In a ketone, there are two factors that make it less likely to undergo a nucleophilic attack than aldehyde. Firstly, the steric hindrance of two carbon groups being attached with the carbonyl carbon makes it harder for the nucleophile to approach. Secondly, the electron push by the carbon groups attached makes the carbonyl carbon a bit less electropositive than the aldehyde one. So aldehydes are more reactive towards a nucleophilic addition reaction.
