Answer:
See figure 1
Explanation:
On this case we have a <u>base</u> (methylamine) and an <u>acid</u> (2-methyl propanoic acid). When we have an acid and a base an <u>acid-base reaction </u>will take place, on this specific case we will produce an <u>ammonium carboxylate salt.</u>
Now the question is: <u>¿These compounds can react by a nucleophile acyl substitution reaction?</u> in other words <u>¿These compounds can produce an amide? </u>
Due to the nature of the compounds (base and acid), <u>the nucleophile</u> (methylamine) <u>doesn't have the ability to attack the carbon</u> of the carbonyl group due to his basicity. The methylamine will react with the acid-<u>producing a positive charge</u> on the nitrogen and with this charge, the methylamine <u>loses all his nucleophilicity.</u>
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Not so sure but i think neon
Answer:
i can't understand the question
Biuret reagent will indicate the presence of protein in a given sample. It is also known as the Piotrowski's test. This reagent consists of copper (II) sulfate and sodium hydroxide. It detects peptide bonds by the reaction of the copper ions in an alkaline solution. The copper ions would form violet colored complexes when peptide is present in the solution. From this test, concentration can be calculated since the intensity of the color depends on the amount of peptide bonds and according to the Beer-Lambert law concentration and the absorption of light is proportional. The concentration is calculated by a spectrophotometric technique at a wavelength of 540 nm.
The narrator is a female
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