Answer:
The soup that is not too hot to eat would be better
Explanation:
because the flavours would be fresher than if it is leftover
Answer:
Measuring with a ruler and using final volume minus initial volume
Explanation:
You can measure the volume of a geometric object by measuring its sides with a ruler and calculating the volume according to the corresponding formula for each object. For example, for a rectangular prism it would be

You can also measure the volume of an object by measuring how much water it displaces. To do this you have to fill a measuring cylinder with enough water for the object to be completely submerged and take note of the volume. Then, add the object and note again the volume of the water+object. The difference between both is the volume of the object.

The advantage of the second method is that it can be used for objects with irregular shapes as long as they do not float.
Answer:
a. Gly-Lys + Leu-Ala-Cys-Arg + Ala-Phe
b. Glu-Ala-Phe + Gly-Ala-Tyr
Explanation:
In this case, we have to remember which peptidic bonds can break each protease:
-) <u>Trypsin</u>
It breaks selectively the peptidic bond in the carbonyl group of lysine or arginine.
-) <u>Chymotrypsin</u>
It breaks selectively the peptidic bond in the carbonyl group of phenylalanine, tryptophan, or tyrosine.
With this in mind in "peptide a", the peptidic bonds that would be broken are the ones in the <u>"Lis"</u> and <u>"Arg"</u> (See figure 1).
In "peptide b", the peptidic bond that would be broken is the one in the <u>"Phe"</u> (See figure 2). The second amino acid that can be broken is <u>tyrosine</u>, but this amino acid is placed in the <u>C terminal spot</u>, therefore will not be involved in the <u>hydrolysis</u>.
The following reaction gives a product with the molecular formula C₄H₈O₂. The diagram of the structure of the product can be seen in the image attached below.
The reaction between C₂H₂(ONa)₂ and C₂H₄Br results in the formation of the product C₄H₈O₂ and 2NaBr.
This reaction undergoes an SN₂ mechanism since there is no stable carbocation formed. In the reaction -O⁻Na⁺ attacks the ortho position in C₂H₄Br to form C₄H₈O₂.
In SN₂ mechanism is a nucleophilic substitution reaction where one bond is formed while another one is broken simultaneously.
The mechanism for the reaction can be seen in the image attached below.
Learn more about nucleophilic substitution reaction here:
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If by classical you mean formula name it is CrPO4<span>.</span>