For an aqueous solution of MgBr2, a freezing point depression occurs due to the rules of colligative properties. Since MgBr2 is an ionic compound, it acts a strong electrolyte; thus, dissociating completely in an aqueous solution. For the equation:
ΔTf<span> = (K</span>f)(<span>m)(i)
</span>where:
ΔTf = change in freezing point = (Ti - Tf)
Ti = freezing point of pure water = 0 celsius
Tf = freezing point of water with solute = ?
Kf = freezing point depression constant = 1.86 celsius-kg/mole (for water)
m = molality of solution (mol solute/kg solvent) = ?
i = ions in solution = 3
Computing for molality:
Molar mass of MgBr2 = 184.113 g/mol
m = 10.5g MgBr2 / 184.113/ 0.2 kg water = 0.285 mol/kg
For the problem,
ΔTf = (Kf)(m)(i) = 1.86(0.285)(3) = 1.59 = Ti - Tf = 0 - Tf
Tf = -1.59 celsius
Here, we should use combined gas law which can be derived from combined gas law, “PV=nRT”. Rearranging, we can get PV/T=nR. Then we can set the two states in the problem together to get
P1V1/T1 = P2V2/T2
Then just plug in and solve algebraically.
Hope this helps
I'm not quiet sure...possibly an ionic bond.
Answer:
What happens when it is squeezed is that its volume increases, the pressure of the material increases.
Explanation:
This is due to the fact that the elastic modulus of the sponge is high and withstands broad forces without deforming its structure, since the force is made within the proportional limit of its particles without modifying or permanently deforming them, that is why when stopping doing pressure or force on it its shape returns to being the original, this also happens due to the phenomenon of resilience
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.
