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Mama L [17]
3 years ago
3

Many antacids contain solid calcium carbonate. Explain how antacids with calcium carbonate function.

Chemistry
2 answers:
Svet_ta [14]3 years ago
6 0

Answer:

Neutralising the acid

Explanation:

the acid present in the stomach is HCl therefore the antiacid reacts with the HCl thus neutralising the acid by forming the products which are salt,water and CO2

Romashka [77]3 years ago
5 0

Answer:

Calcium carbonate contains the carbonate ion.

Calcium carbonate accepts free H+ ions.

When an acid reacts with a carbonate, carbon dioxide gas is one of the products.

If antacids are dissolved prior to ingestion, the reaction between carbonate and hydrogen is faster.

Explanation:

From edge2020 :)

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Calculate the molarity of the solution if 80.0 g of Kool-Aid is dissolved in 1.0<br> L of solution.
Serga [27]

Answer:

.234 M

Explanation:

Molarity, or concentration, of a substance is simply found by dividing the amount of that substance in moles by its volume. Here, we are given the mass (in grams) of Kool-Aid, so we need to convert that to moles. To do this, we simply need the chemical formula of Kool-Aid, which I have found to be C12H22O11. The molar mass of C12H22O11, using the periodic table, is 342.296 g. Next, take this molar mass and divide the given mass of Kool-Aid by it. You then get about .234 mol Kool-Aid.

Lastly, divide this by the volume of 1.0 L. You get .234 M as your final molarity.

7 0
3 years ago
What do the symbols in parenthesis indicate? C7H16 (l) + 11O2 (g) 7CO2 (g) + 8H2O (l) the physical state of each reactant and pr
Vadim26 [7]
The symbols indicate the physical state of each reactant
8 0
3 years ago
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Phenol, c6h5oh, is a stronger acid than methanol, ch3oh, even though both contain an o]h bond. Draw the structures of the anions
timurjin [86]

In resonance structures, the chemical connectivity in the molecule is same but the distribution of electrons are different around the structure.  They are created by moving electrons in double or triple bonds, and not atoms.

Phenol, C_6H_5OH and methanol, CH_3OH both are alcohols  that contain an -OH group attached to carbon atom.

Due to loss of 1 H from phenol, it forms phenoxide anion and due to presence of double bond in the benzene ring the negative charge on the oxygen atom (which represents electrons) will resonate with double bonds of benzene ring as shown in the image. The resonance-stabilized phenoxide ion is more stable. Whereas when methanol lose 1 H it forms methoxide anion and there are no such electrons present in the structure of methoxide that will result in the movement of electron. Since, due to resonance-stabilized phenoxide ion is more stable than methoxide ion, so it is a stronger acid.

The structures of the anions resulting from loss of 1 H from phenol and methanol is shown in the image.

8 0
3 years ago
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olga nikolaevna [1]

Answer: 94.07%

Explanation:

Percentage yield can be calculated by the formula

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Theoretical yield = 8.43

%yield = Experimental yield/Theoretical yield x100

%yield = 7.93/8.43 x 100 = 94.07%

4 0
3 years ago
What variables are considered when forecasting weather
saveliy_v [14]
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4 0
3 years ago
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