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Dahasolnce [82]
3 years ago
12

Calculate the % dissociation of 0.10 M solution of acetic acid (pKa = 4.75)

Chemistry
1 answer:
madreJ [45]3 years ago
3 0

Given :

Molarity of acetic acid solution, M = 0.10 M.

pKa of acetic acid, pKa = 4.75 .

To Find :

Percentage dissociation of 0.10 M solution of acetic acid.

Solution :

We know, pK_a = -log\  K_a

Taking antilog both side, we get :

K_a = 1.78\times 10^{-5}

Since, acetic acid has 1 hydrogen atom to loose , so it is a monoprotic acid.

Now, percentage dissociation of monoprotic acid is given by :

\alpha = \sqrt{\dfrac{K_a}{C}}\\\\\alpha =\sqrt{ \dfrac{1.78\times 10^{-5}}{0.1}}\\\\\alpha =  0.0133\times 100 = 1.33 \%

Hence, this is the required solution.

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amm1812

Answer:

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=1 means is 1 or greater so that would be p, d, f, and g subshells

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4 0
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NaCl + H2SO4 ---&gt; Na2SO4 + HCl<br> Balance the double replacement chemical reaction.
VikaD [51]

Answer:

2NaCl+H2SO4-->Na2SO4+2HCl

Explanation:

There are two Na on the right, so put a 2 in front of NaCl on the left. This makes 3 Cl also, so put a 2 in front of HCl on the right. There are already 2 H on the left, so the equation is balanced.

7 0
3 years ago
Select the correct answer.
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Answer:

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Which of the following elements would form the smallest ionic radius and why?
AnnyKZ [126]

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5 0
3 years ago
How can you determine which bond in a structure is more polar without using an electronegativity table?
UkoKoshka [18]
To know this you pretty much do have to kind of memorize a few electronegativities. I don't recall ever getting a table of electronegativities on an exam.
From the structure, you have:

I remember the following electronegativities most because they are fairly patterned:
EN
H
=
2.1
EN
C
=
2.5
EN
N
=
3.0
EN
O
=
3.5
EN
F
=
4.0
EN
Cl
=
3.5
Notice how carbon through fluorine go in increments of
~
0.5
. I believe Pauling made it that way when he determined electronegativities in the '30s.
Δ
EN
C
−
Cl
=
1.0
Δ
EN
C
−
H
=
0.4
Δ
EN
C
−
C
=
0.0
Δ
EN
C
−
O
=
1.0
Δ
EN
O
−
H
=
1.4
So naturally, with the greatest electronegativity difference of
4.0
−
2.5
=
1.5
, the
C
−
F
bond is most polar, i.e. that bond's electron distribution is the most drawn towards the more electronegative compound as compared to the rest.
When the electron distribution is polarized and drawn towards a more electronegative atom, the less electronegative atom has to move inwards because its nucleus was previously favorably attracted to the electrons from the other atom.
That means generally, the greater the electronegativity difference between two atoms is, the shorter you can expect the bond to be, insofar as the electronegative atom is the same size as another comparable electronegative atom.
However, examining actual data, we would see that on average, in conditions without other bond polarizations occuring:
r
C
−
Cl
≈
177 pm
r
C
−
C
≈
154 pm
r
C
−
O
≈
143 pm
r
C
−
F
≈
135 pm
r
C
−
H
≈
109 pm
r
O
−
H
≈
96 pm
So it is not necessarily the least electronegativity difference that gives the longest bond.
Therefore, you cannot simply consider electronegativity. Examining the radii of the atoms, you should notice that chlorine is the biggest atom in the compound.
r
Cl
≈
79 pm
r
C
≈
70 pm
r
H
≈
53 pm
r
O
≈
60 pm
So assuming the answer is truly
C
−
C
, what would have to hold true is that:
The
C
−
F
bond polarization makes the carbon more electropositive (which is true).
The now more electropositive carbon wishes to attract bonding pairs from chlorine closer, thereby shortening the
C
−
Cl
bond, and potentially the
C
−
H
bond (which is probably true).
The shortening of the
C
−
Cl
bond is somehow enough to be shorter than the
C
−
C
bond (this is debatable).
5 0
4 years ago
Read 2 more answers
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