A buffer is simply a mixture of a weak acid and its conjugate base or a weak base and its conjugate acid. Buffers work by reacting with any added acid or base to control the pH.
Hope this helps
Explanation:
Environment conservation is an umbrella term that defines anything we do to protect our planet and conserve its natural resources so that every living thing can have an improved quality of life. bolivianouft and 7 more users found this answer helpful.
Answer:
7.5 L of the 10% and 22.5 L of the 30% acid solution, she should mix.
Explanation:
Let the volume of 10% acid solution used to make the mixture = x L
So, the volume of 30% acid solution used to make the mixture = y L
Total volume of the mixture = <u>x + y = 30 L .................. (1)
</u>
For 10% acid solution:
C₁ = 10% , V₁ = x L
For 30% acid solution :
C₂ = 30% , V₂ = y L
For the resultant solution of sulfuric acid:
C₃ = 25% , V₃ = 30 L
Using
C₁V₁ + C₂V₂ = C₃V₃
10×x + 30×y = 25×30
So,
<u>x + 3y = 75 .................. (2)
</u>
Solving 1 and 2 we get,
<u>x = 7.5 L
</u>
<u>y = 22.5 L</u>
It is covalent bonding. The electrons are shared between the phosphorus and the chlorines.
covalent bonding is when electrons are shared between two elements.
molecular polarity is a little bit complicated, but I will try to explain ;)
PCl3 is an alternation on tetrahedral molecules.
It means that P has one lone pair of electrons. This pair of electrons are only attracted to the P nuclei and thus a greater freedom of motion.
This means that their orbital is bigger and this pushes the 3 Cl atoms closer together.
The angle between each Cl now is 107 and the angle between Cls and P is greater than 107.
Now, due to this shape, and also electronegativity (Cl is more electronegative than P meaning that it tends to hog the electrons they share closer to itself), PCl3 is polar. Electrons that are shared tend to flow closer towards the Cl than the P side.
Therefore, on the Cl side of the molecule it's, more negative. On the P side, it's more positive.
Acetone has α-hydrogens (on both sides) and thus can be deprotonated to give a nucleophilic enolate anion. The aldehyde carbonyl is much more electrophilic than that of a ketone, and therefore reacts rapidly with the enolate.
<h3>What is nitrobenzaldehyde?</h3>
- Synthesis. The synthesis of 3-nitrobenzaldehyde is achieved via nitration of benzaldehyde, which yields especially the meta-isomer. Creation allocation is about 19% for the ortho-, 72% for the meta- and 9% for the para isomers.
- Acetone, propanone, or dimethyl ketone, is an organic combination with the formula (CH3)2CO. It is the easiest and smallest ketone. It is a colorless, highly volatile, and combustible liquid with a characteristic aromatic odor.
- Nitration of benzene with conc nitric acid and conc sulphuric acid gives nitrobenzene. Chlorination with chlorine in the existence of anhydrous aluminum chloride gives meta nitro chlorobenzene.
To learn more about sulphuric acid, refer to:
brainly.com/question/4018599
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