Solution :
Comparing the solubility of silver chromate for the solutions :
----- Less soluble than in pure water.
----- Less soluble than in pure water.
----- Similar solubility as in the pure water
----- Similar solubility as in the pure water
The silver chromate dissociates to form :
When 0.1 M of 
is added, the equilibrium shifts towards the reverse direction due to the common ion effect of 
, so the solubility of 
decreases.
Both 
and 
are neutral mediums, so they do not affect the solubility.
Any substance changes to another substance that means the change of the physical property. Like water () has different state which changes as the temperature changes. It remain as liquid in the room temperature, in solid form at or below 0°C and vapor phase on or above 100°C. But in all the stage or phase of the substance the composition of the water i.e. remains. Thus the chemical property remains fixed when a substance change to other substance.
Answer:
I would expect the gas rate determined in this manner to be too low
Explanation:
A Rotameter can be designed to respond to the sensitivity of density, velocity, to measure the flow rate of liquid or gas enclosed in a tube. Liquids are denser than gas, and since the gas rate to be determined needed to respond to the velocity head alone of the rotameter so as to bring the forces in the tube equilibrium. Knowing if there is no flow, then the float would remain at the bottom, so gas has to flow at a higher rate compared to the liquid so the float would be in a similar position making it easier to measure the flowrate. This leaves the gas rate to be determined too low.
Answer:
Product: ethyl L-valinate
Explanation:
If we want to understand what it is the molecule produced we have to an<u>alyze the reagents</u>. We have valine an <u>amino acid</u>, in this kind of compounds we have an <em>amine group</em> (
) and a <em>carboxylic acid</em> group (
). Additionally, we have an <u>alcohol </u>(
) in the presence of HCl (a <u>strong acid</u>) in the first step, and a base (
).
When we have an acid and an alcohol in a vessel we will have an <u>esterification reaction</u>. In other words, an ester is produced. As the <em>first step,</em> the oxygen in the C=O (in the carboxylic acid group) would be protonated. In the <em>second step</em>, the ethanol attacks the carbon in the C=O of the carboxylic acid group producing a new bond between the oxygen in the ethanol and the carbon in the carboxylic acid. In <em>step 3</em>, a proton is transferred to produce a better leaving group (
). In <em>step 4</em>, a water molecule leaves the main structure to produce again the double bond C=O. <em>Finally</em>, a base () removes the hydrogen from the C=O bond to produce ethyl L-valinate
See figure 1
I hope it helps!
