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Natalija [7]
2 years ago
14

What are the products of the neutralization reaction between HCl and

Chemistry
1 answer:
liraira [26]2 years ago
4 0

Answer:

opinion b

Explanation:

the product of neutralization reaction between hcl and CA(oh)2 is option b.

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What is the percent by volume of isopropyl alcohol in a solution that contains 45 ml of isopropyl alcohol in 1.4 L of water?
11Alexandr11 [23.1K]

Answer:

3.11%

Explanation:

We express a solution's volume by volume percent concentration, % v/v,

Take the ratio of the isopropyl alcohol (IPA) volume to the total volume of the solution, which is 1400 mL of water+ 45 mL of IPA,

and multiply by 100 to get the percentage:    45/(1400+45) *100 = 0.0311*100 =  3.11%

6 0
3 years ago
What is the IUPAC name for this product?
mihalych1998 [28]

The IUPAC name for the given product is 2 chloro Butane.

<h3>What is IUPAC nomenclature?</h3>

IUPAC stands for 'International Union of Pure and Applied Chemistry', which givers some rule for designing the name of compounds of chemistry.

  • In the given product total four carbon atoms are present and between all of them single bonds are present.
  • In the second carbon atom, chlorine group is present.
  • During the nomenclature process, first we write down the name of the attached group which is followed by the alkane chain.

Hence name of the product is 2 chloro Butane.

To know more about IUPAC nomenclature, visit the below link:

brainly.com/question/26635784

#SP1

7 0
2 years ago
In Chromium-53, the "53" represents the
alina1380 [7]

Answer:

The differemt isotopes that differ in atomic mass

Explanation:

4 0
2 years ago
Read 2 more answers
What are the chemical processes used to make chloroquine?
4vir4ik [10]
You spell Chlorine wrong but the process is called electrolysis  
6 0
3 years ago
The aldol reaction is catalyzed by acid as well as base. What is the reactive nucleophile in the acid-catalyzed aldol reaction
svp [43]

Answer:

The reactive nucleophile is Ketone.

Explanation:

In organic chemistry, The process of acid - catalyzed aldol condensation starts from when ketone (or any aldehyde) is converted to an -enol, after which it attacks another ketone/aldehyde that has already been activated by parbonyl oxygen protonation.

The process of this is that first of all the ketone undergoes tautomerization to form -enol. Thereafter, the other carbonyl will undergo protonation which makes the carbon activated towards attack. Now, the nucleophilic enol will be added to the carbonyl in a [1,2]-addition reaction and we will now use deprotonation to obtain the neutral Aldol product.

Now, since only the ketone can produce an -enol, thus it is the nucleophile as aldehydes are better electrophiles

4 0
3 years ago
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