Answer:
A. the burning of fossil fuels within the Sun
Explanation:
Answer: Secondary amines react with the nitrosonium ion to generate <span>
<u>N-Nitrosoamines</u>.
Explanation: Nitosonium Ion is generally utilized in the formation of
Diazonium Salts which are considered excellent starting Material from synthesis point of View. Diazonium salts are formed by reacting
Primary Amine or
Anilines with Nitrosonium Ions. In our case, the Amine given is Secondary. So, reaction of <em>Sec.</em> Amines with Nitrosonium Ions stops after the formation of N-Nitrosoamine as there is no Hydrogen attached to Nitrogen atom of Amine to be eliminated and form a double and eventually triple bond with the Nitrogen atom of Nitrosonium Ion.</span>
During transpeptidation, nucleophilic attack occurs between the α-amine group in the A site and the esterified carbon in the P site
<h3>What is transpeptidation ?</h3>
A chemical process in which an amino acid residue or peptide residue is transferred from one amino compound to another. This process occurs when a protease reversibly converts one peptide to another.
- a process where one or more amino acids are transferred from one peptide chain to another, as in the case of a transpeptidase activity, or where a peptide chain itself is produced, as in the case of the production of a bacterial cell wall.
- Peptidoglycan glyco-syltransferases create the glycan strands (PGTs). The most popular class of antibiotics' fatal targets are enzymes termed transpeptidases (TPs), which produce the peptide crosslinks: using beta-lactams
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