Sugar dissolves faster in hot water than it does in cold water because hot water has more energy than cold water. when water is heated, the molecules gain energy and because of that, move faster. as they move faster, they come in contact with the sugar more often, causing it to dissolve faster.
Answer:
Explanation:
From the given information:
The equation for the reaction can be represented as:
The I.C.E table can be represented as:
2SO₂ O₂ 2SO₃
Initial: 14 2.6 0
Change: -2x -x +2x
Equilibrium: 14 - 2x 2.6 - x 2x
However, Since the amount of sulfur trioxide gas to be 1.6 mol.
SO₃ = 2x,
then x = 1.6/2
x = 0.8 mol
For 2SO₂; we have 14 - 2x
= 14 - 2(0.8)
= 14 - 1.6
= 12.4 mol
For O₂; we have 2.6 - x
= 2.6 - 1.6
= 1.0 mol
Thus;
[SO₂] = moles / volume = ( 12.4/50) = 0.248 M ,
[O₂] = 1/50 = 0.02 M ,
[SO₃] = 1.6/50 = 0.032 M
Kc = [SO₃]² / [SO₂]² [O₂]
= ( 0.032²) / ( 0.248² x 0.02)
= 0.8325
Recall that; the equilibrium constant for the reaction = 0.8325;
If we want to find:
Then:
Since no temperature is given to use in the question, it will be impossible to find the final temperature of the mixture.
Answer:
Mostly Para
Explanation:
First, let's assume that the molecule is the toluene (A benzene with a methyl group as radical).
Now the nitration reaction is a reaction in which the nitric acid in presence of sulfuric acid, react with the benzene molecule, to introduce the nitro group into the molecule. The nitro group is a relative strong deactiviting group and is metha director, so, further reactions that occur will be in the metha position.
Now, in this case, the methyl group is a weak activating group in the molecule of benzene, and is always ortho and para director for the simple fact that this molecule (The methyl group) is a donor of electrons instead of atracting group of electrons. Therefore for these two reasons, when the nitration occurs,it will go to the ortho or para position.
Now which position will prefer to go? it's true it can go either ortho or para, however, let's use the steric hindrance principle. Although the methyl group it's not a very voluminous and big molecule, it still exerts a little steric hindrance, and the nitro group would rather go to a position where no molecule is present so it can attach easily. It's like you have two doors that lead to the same place, but in one door you have a kid in the middle and the other door is free to go, you'll rather pass by the door which is free instead of the door with the kid in the middle even though you can pass for that door too. Same thing happens here. Therefore the correct option will be mostly para.
Answer:
what type of question?
Explanation:
whats your favorite color???
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