Answer:
The volume (mL) of 0.135 M NaOH that is required to neutralize 13.7 mL of 0.129 M HCl is 13.1 mL (option b).
Explanation:
The reaction between an acid and a base is called neutralization, forming a salt and water.
Salt is an ionic compound made up of an anion (positively charged ion) from the base and a cation (negatively charged ion) from the acid.
When an acid is neutralized, the amount of base added must equal the amount of acid initially present. This base quantity is said to be the equivalent quantity. In other words, at the equivalence point the stoichiometry of the reaction is exactly fulfilled (there are no limiting or excess reagents), therefore the numbers of moles of both will be in stoichiometric relationship. So:
V acid *M acid = V base *M base
where V represents the volume of solution and M the molar concentration of said solution.
In this case:
- V acid= 13.7 mL= 0.0137 L (being 1,000 mL= 1 L)
- M acid= 0.129 M
- V base= ?
- M base= 0.135 M
Replacing:
0.0137 L* 0.129 M= V base* 0.135 M
Solving:

V base=0.0131 L = 13.1 mL
<u><em>
The volume (mL) of 0.135 M NaOH that is required to neutralize 13.7 mL of 0.129 M HCl is 13.1 mL (option b).</em></u>
I think it’s 5000 because it says that their is over 4,124 valid species of minerals.
Answer:
I think B but I'm not sure.
Answer:
Decay-the breakdown of dead plants..
Earth- thermal energy comes from deep inside...
Fires- these consume feul...
Explanation:
Complete Question:
check the first image for complete part of the question
Answer and Explanation:
Epoxide is a three membered ring made up of two carbon atoms and one oxygen atom. Epoxides are cyclic ethers. Due to its ring size, it is highly strained and very reactive. Epoxide ring opening takes place with respect to addition of acid and base.
Ring opening of epoxide with acid:
In the presence of base, the nucleophile attacks the epoxide ring at more substituted site and inverse stereochemistry takes place.(check file 2 attached)
Ring opening of epoxide with base:
The backside attack of nucleophile takes place in less substituted site and then it undergoes protonation to form a product.
(check file 2 attached)