Answer:
a)
⇒
⇒
b)
⇒
⇒
Explanation:
A)
Remember that positive number superscripts mean electrons lack and negative numbers mean electrons 'excess' (if we compare it with the neutral element). So, for the case of Fe2+ which is converted to Fe3+, we know that in Fe2+ there is a two electrons lack, while in Fe3+ there is a 3 electrons lack; it means that Fe2+ was converted to Fe3+ but releasing one electron:
⇒
The same analysis is applied to Br2; Br2 is a molecule which is said to have a zero superscript because it is an apolar covalent bond; and it is converted to Br-, which, according to what I wrote above, means that there is a one electron excess. So, Br2 must have received an electron in order to change to Br-; but Br2 can't change to Br- as simple as that because Br2 is a molecule, not an atom; it is a molecule that has two Br atoms, so, Br2 must give two Br- ions as products, but receiving one electron for each one:
⇒
b)
Applying the same, in Mg2+ there is a 2 electrons lack, and in Mg is not electron lack (its superscript is zero), so Mg must have released two electrons in order to change to Mg2+:
⇒
Cr3+ has a 3 electrons lack, and Cr2+ a two electrons one, so, Cr3+ must receive an electron to convert to Cr2+:
⇒
Answer: dilute
Explanation:
A concentrated solution which is used to prepare solutions of lower concentrations by diluting it with addition of water.
A dilute solution is one which contains lower concentration.
Using Molarity equation:
=concentration of stock solution = 0.150 mol/L
= volume of stock solution = 10.0 ml
= concentration of dilute solution = ?
= volume of dilute solution = (10.0+90.0) ml = 100.0 ml


As the concentration is less than the original concentration, the solution is termed as dilute.
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.