<span>It's because the product formed with BF3 is more complex which able to decompose AlF3.
</span>AlF3 doesn't dissolve in HF because of the fluorine. It's doesn't allow for coordination due to the hydrogen. However, it will dissolve in KF. If you look at the chemical reaction, it's able to form a salt.
<span>3KF+Al<span>F3</span>−>3KF.Al<span>F3</span></span>
Answer:
HPRT
Explanation:
HPRT catalyzes the salvage reactions of hypoxanthine and guanine with PRPP to form IMP and GMP
The formation of GMP from IMP requires oxidation at C-2 of the purine ring, followed by a glutamine-dependent amidotransferase reaction that replaces the oxygen on C-2 with an amino group to yield 2-amino,6-oxy purine nucleoside monophosphate, or as this compound is commonly known, guanosine monophosphate.
The emission of the light waves ..................... which means that THE TROUGHS OF ONE WAVE AND THE CREST OF ANOTHER overlap.
When the trough and the crest of wave overlap, it results in constructive interference and the amplitude of the two waves are added together to form a larger amplitude.<span />
Answer:
Kc = 3.90
Explanation:
CO reacts with
to form
and
. balanced reaction is:

No. of moles of CO = 0.800 mol
No. of moles of
= 2.40 mol
Volume = 8.00 L
Concentration = 
Concentration of CO = 
Concentration of
= 

Initial 0.100 0.300 0 0
equi. 0.100 -x 0.300 - 3x x x
It is given that,
at equilibrium
= 0.309/8.00 = 0.0386 M
So, at equilibrium CO = 0.100 - 0.0386 = 0.0614 M
At equilibrium
= 0.300 - 0.0386 × 3 = 0.184 M
At equilibrium
= 0.0386 M
![Kc=\frac{[H_2O][CH_4]}{[CO][H_2]^3}](https://tex.z-dn.net/?f=Kc%3D%5Cfrac%7B%5BH_2O%5D%5BCH_4%5D%7D%7B%5BCO%5D%5BH_2%5D%5E3%7D)

Answer:
See explanation and images attached
Explanation:
a) In the mechanism for the acid catalysed esterification of propanoic acid using ethanol, we can see that the first step is the protonation of the acid followed by nucleophillic attack of the alcohol. Loss of water and consequent deprotonation regenerates the acid catalyst. We can see the fate of the 18O labelled ethanol in the mechanism shown.
b) In the second mechanism, an unnamed ester is hydrolysed using an acid catalyst. The attack of the acid and subsequent nucleophillic attack of water labelled with 18O leads to the incorporation of this 18O into the product acid as shown in the mechanism attached to this answer.