Answer:
I attached the answer as an image. I also drew in the two most acidic hydrogens.
Explanation:
This goes through the 'benzyne' intermediate, meaning it does an E2-looking reaction by expelling a leaving group (chloride) from the adjacent part of the ring using the amide as a strong base. The triple-bonded benzyne has absurd bond angle strain, and is vulnerable to a good nucleophile like an amide ion, and the resultant sp2 anion is then reprotonated by the acid. I didn't draw in the acid-base reaction in step one, or the spectator ion (sodium).
Answer:b
Explanation: it’s in the picture just go counterclockwise
If you can't answer a question, then make an educated guess.
A cation-exchange column is a type of chromatography that separates substances according to their charges. The cation-exchange column in particular has a negatively charged resin that will attract positively charged ions.
Applying this principle with amino acids, we can say, for example that the negatively charged ones (e.g., aspartate and glutamate) will elute first compared to the positively charged ones (e.g., lysine, arginine, and histidine), which will elute last.
When an atom or molecule accepts or looses an electron or electrons it gets either negative charge (when electrons gained) or a positive charge (when looses electron). The negative ion is called Anion and positve ion is called the Cation. An Ion can be Atomic or Polyatomic.
Example:
Sodium when looses one electron forms a cation i.e. Na⁺
Chlorine when gains one electron forms an Anion i.e. Cl⁻
Result:
<span>A negative ion (Anion) differ from an uncharged atom of the same element in the number of electrons. An anion contains more electrons than its corresponding Neutral Element.</span>
