10 points Part F

Chemistry

1 answer:

Arisa [49]3 years ago

5 0

Answer and Explanation:

When using simulations, it is important that the researcher knows some limitations. This is because the simulations do not behave exactly like what they represent, in addition to not presenting very important details for analysis and without approximations of what really happens with what they are representing. When modeling the synthesis of Ammonia, for example, these limitations can cause inaccuracies that will compromise the entire analysis.

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Choose all the answers that apply.

zmey [24]

Calcium is a non metal

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3 years ago

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Enzymes in the small intestine break down proteins, carbohydrates, and lipids. These enzymes are named after the substrate they

svetoff [14.1K]

The enzymes and their respective substrates are as follows:

Protease enzymes such as trypsin and chymotrypsin break down proteins
Carbohydrate enzymes such amylase and maltase break down carbohydrates
Lipase enzyme breaks down lipids.

In the small intestine, a protease enzyme known as chymotrypsin breaks down protein, pancreatic amylase breaks down carbohydrates, while pancreatic lipase breaks down lipids.

More on biological enzymes can be found here: brainly.com/question/12194042

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2 years ago

choose any bases that will selectively deprotonate the above acid, that is, any bases that will favor the formation of products.

Zanzabum

In order to deprotonate an acid, we must remove protons in order to achieve a more stable conjugate base. For this example, we can use the relationship between carboxylic acid and hydroxide.

Deprotonation is the removal of a proton from a specific type of acid in reaction to its coming into contact with a strong base. The compound formed from this reaction is known as the conjugate base of that acid. The opposite process is also possible and is when a proton is added to a special kind of base. This is a process referred to as protonation, which forms the conjugate acid of that base.

For the example we have chosen to give, the conjugate base is the carboxylate salt. This would be the compound formed by the deprotonated carboxylic acid. The base in question was strong enough to deprotonate the acid due to the greater stability offered as a conjugated base.

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