Nitrous acid<span> dissociates as follows:
</span>
HNO₂(s) ⇄ H⁺(aq) + NO₂⁻(aq)
According to the equation, an acid constant has the following form:
Ka = [H⁺] × [NO₂⁻ ] / [HNO₂]
From pH, we can calculate the concentration of H⁺ and NO₂⁻:
[H⁺] = 10^-pH = 10^-2.63 = 0.00234 M = [NO₂⁻]
Now, the acid constant can be calculated:
Ka = 0.00234 x 0.00234 / 0.015 = 3.66 x 10⁻⁴
And finally,
pKa = -log Ka = 3.44
Answer: The substance is neutral
Explanation:
If you place red litmus paper into a basic substance, it turn's blue. When it comes in contact with an acidic or neutral substance, it doesn't change colour it remains red.
Blue litmus paper in acid turns red when placed in a basic or neutral solution it remains blue. From this it can be concluded that the solution is neutral.
Answer: balanced chemical equation: 
Net ionic equation :
Explanation:
A double displacement reaction is one in which exchange of ions take place. The salts which are soluble in water are designated by symbol (aq) and those which are insoluble in water and remain in solid form are represented by (s) after their chemical formulas.
The balanced chemical equation is:

Spectator ions are defined as the ions which does not get involved in a chemical equation or they are ions which are found on both the sides of the chemical reaction present in ionic form.
The ions which are present on both the sides of the equation are sodium and nitrate ions and hence are not involved in net ionic equation.
Hence, the net ionic equation is
<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.