None of the choices are right
Answer:
See detailed mechanism in the image attached
Explanation:
The mechanism shown in detail below is the synthesis of serine in steps.
The first step is the attack of the ethoxide ion base on the diethyl acetamidomalonate substrate giving the enolate and formaldehyde.
The second step is the protonation of the oxyanion from (1) above to form an alcohol as shown.
Acid hydrolysis of the alcohol formed in (3) above yields a tetrahedral intermediate, a dicarboxyamino alcohol.
Decarboxylation of this dicarboxyamino alcohol yields serine, the final product as shown in the image attached.
2K2MnO4 + Cl2 -------> 2KMnO4 + 2KCl
Answer:
A compound is just pure that is composed of elements that are chemically bonded in definite proportions
andd solution is umm well its a homogenous so basically saying
that it all just stays the same all the way through
Explanation:
im not sure how else to explain it haah hope this helped :P
Answer:
studies
Explanation:
if they get plenty of studies then they get it