Answer:
The answer is Denaturation is reversible
Explanation:
Denaturation of proteins is the process whereby there is a disruption in the tertiary, quaternary or secondary structure of proteins which causes a conformation change in its action
denaturation is reversible, that is, the proteins can regain their native state when the denaturing influence is removed. This process can be called renaturation.
Answer:
Explanation:
When the amount of H2O2 is doubled while KI is kept constant, the rate of reaction doubles.
When the amount of KI is doubled and the amount of H2O2 is halved, the rate stays nearly constant.
2H2O2 (aq) → O2(g) + 2H2O (l) ------------- first order kinetics reaction.
Catalysts are KI, FeCl3 only, KCl is not a catalyst. Order: KI < MnO2 < Pb < FeCl3.
H2O2 + I– -> IO– + H2O (Step 1)
H2O2 + IO– -> I– + H2O + O2 (Step 2)
It can be seen that the iodine ion (provided by the KI solution) is a product as well as a reactant.
02(g)2Fe? (aq) + 2 H(a) 2 H 2 Fe3 (aq) H2O2(aq) + 2 Fe,Taq) H02(aq) 2 Fe (aq) 2 H (aq)
Answer:
Biphenyl
Explanation:
The reaction of bromo benzene with magnesium-ether solution yields a Grignard reagent.
The byproduct of this reaction is biphenyl. It is formed when two unreacted bromobenzene molecules are coupled together.
Hence, It is advised that the bromobenzene solution be added slowly to the magnesium-ether solution so that it isn't present in a high concentration, thus reducing the amount of biphenyl by-product formed.
Answer:
A beaker
Step-by-step explanation:
Specifically, I would use a 250 mL graduated beaker.
A beaker is appropriate to measure 100 mL of stock solution, because it's easy to pour into itscwide mouth from a large stock bottle.
You don't need precisely 100 mL solution.
If the beaker is graduated, you can easily measure 100 mL of the stock solution.
Even if it isn't graduated, 100 mL is just under half the volume of the beaker, and that should be good enough for your purposes (you will be using more precise measuring tools during the experiment).