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Ipatiy [6.2K]
4 years ago
12

A 100 ml graduated cylinder with an inside diameter of 3.2 cm contains 34.0 g of gasoline and 34.0 g of water. what is the combi

ned height of the two liquid layers
Chemistry
1 answer:
Ivahew [28]4 years ago
3 0

The volume of cylinder is 100 mL, inner diameter is 3.2 cm thus, radius will be:

r=\frac{d}{2}=\frac{3.2 cm}{2}=1.6 cm

Volume of layer formed=\pi r^{2}h...... (1)

Volume of layer is also equal to sum of volume of gasoline and water.

Density of gasoline is 0.702 g/cm^{3} and mass is 34 g thus, volume of gasoline will be:

V=\frac{m}{d}=\frac{34 g}{0.702 g/cm^{3}}=48.43 cm^{3}

Now, density of water is 1 g/cm^{3} and mass is 34 g thus, volume of water will be:

V=\frac{m}{d}=\frac{34 g}{1 g/cm^{3}}=34 cm^{3}

Adding both the volumes, volume of layer will be:

Volume of layer=48.43 cm^{3}+34 cm^{3}=82.43cm^{3}

Putting the values in equation (1) to solve for height of the layer,

h=\frac{volume of layer}{\pi r^{2}}=\frac{82.43 cm^{3}}{3.14\times 1.6 cm\times 1.6 cm}=10.25 cm

Thus, height of layer is 10.25 cm

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Explanation:

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What effect does cutting down forests have on the carbon dioxide levels in the atmosphere?
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5 0
3 years ago
Convert the following Celsius temperatures to the Kelvin scales
kotykmax [81]
What are the temperatures
5 0
3 years ago
I begin the reaction with 0.45 g of beryllium. If my actual yield of beryllium chloride (mm = 79.91 g/mol) was 3.5 grams, what w
trasher [3.6K]

The percentage of yield was 777.78%

<u>Explanation:</u>

We have the equation,

Be [s]  +  2 HCl [aq]  →  BeCl 2(aq]  + H 2(g]  ↑ Be (s]  + 2 HCl [aq]  →  BeCl 2(aq]  + H 2(g] ↑

To find the percent yield we have the formula

Percentage of Yield= what you actually get/ what you should theoretically get  x 100

                                   =3.5 g/0.45 g 100

                                    = 777.78 %

The percentage of yield was 777.78%

5 0
4 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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