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shtirl [24]
2 years ago
7

A 20.0–milliliter sample of 0.200–molar K2CO3 so­lution is added to 30.0 milliliters of 0.400–mo­lar Ba(NO3)2 solution. Barium c

arbonate precipi­tates. The concentration of barium ion, Ba2+, in solution after reaction is_________.
Chemistry
1 answer:
iragen [17]2 years ago
6 0

Answer:

[Ba^2+] = 0.160 M

Explanation:

First, let's calculate the moles of each reactant with the following expression:

n = M * V

moles of K2CO3 = 0.02 x 0.200 = 0.004 moles

moles of Ba(NO3)2 = 0.03 x 0.400 = 0.012 moles

Now, let's write the equation that it's taking place. If it's neccesary, we will balance that.

Ba(NO3)2 + K2CO3 --> BaCO3 + 2KNO3

As you can see, 0.04 moles of  K2CO3 will react with only 0.004 moles of Ba(NO3) because is the limiting reactant. Therefore, you'll have a remanent of

0.012 - 0.004 = 0.008 moles of Ba(NO3)2

These moles are in total volume of 50 mL (30 + 20 = 50)

So finally, the concentration of Ba in solution will be:

[Ba] = 0.008 / 0.050 = 0.160 M

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In two or more complete sentences describe all of the van der Waals forces that exist between molecules of sulfur
zavuch27 [327]

Answer:

Dipole-Dipole attraction

Explanation:

Dipole-dipole attraction is a type of vander waals forces found in the molecules of sulfur dioxide.

Vander waals forces are weak attractions joining non-polar and polar molecules together. They are of two types:

  • London dispersion forces which are weak attractions found between non-polar molecules.
  • Dipole-Dipole attraction are the forces of attraction which exists between polar molecules. Such molecules have permanent dipoles. This implies that the positive pole of one molecule attracts the negative pole of another. This is what happens between the oxygen and sulfur molecules.
3 0
2 years ago
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How many hydrogen bonds can CH2O make to water
VladimirAG [237]
Hydrogen bonds are not like covalent bonds. They are nowhere near as strong and you can't think of them in terms of a definite number like a valence. Polar molecules interact with each other and hydrogen bonds are an example of this where the interaction is especially strong. In your example you could represent it like this: 

<span>H2C=O---------H-OH </span>

<span>But you should remember that the H2O molecule will be exchanging constantly with others in the solvation shell of the formaldehyde molecule and these in turn will be exchanging with other H2O molecules in the bulk solution. </span>

<span>Formaldehyde in aqueous solution is in equilibrium with its hydrate. </span>

<span>H2C=O + H2O <-----------------> H2C(OH)2</span>
5 0
2 years ago
Write a hypothesis for this: Hummingbirds are attracted to the color red
Margaret [11]

Answer: I believe/don't believe hummingbirds are attracted to the color red because ... (Enter your reasons)

Explanation:

Hypothesis are always different, up to you to choose believe or not believe depending on your position.

:) Hope this helped.

8 0
2 years ago
Consider the skeletal structure of naphthalein (C10H8), the active ingredient in mothballs. How many double bonds must be added
Greeley [361]

Answer:

four (4)

Explanation:

Naphthalein is an organic compound with formula C 10H 8. It is the simplest polycyclic aromatic hydrocarbon, and is a white crystalline solid with a characteristic odor that is detectable at concentrations as low as 0.08 ppm by mass. As an aromatic hydrocarbon, naphthalene's structure consists of a fused pair of benzene rings. It is best known as the main ingredient of traditional mothballs.

The molecule is planar, like benzene. Unlike benzene, the carbon–carbon bonds in naphthalene are not of the same length. The bonds C1−C2, C3−C4, C5−C6 and C7−C8 are about 1.37 Å (137 pm) in length, whereas the other carbon–carbon bonds are about 1.42 Å (142 pm) long. This difference, established by X-ray diffraction is consistent with the valence bond model in naphthalene and in particular, with the theorem of cross-conjugation. This theorem would describe naphthalene as an aromatic benzene unit bonded to a diene but not extensively conjugated to it (at least in the ground state), which is consistent with two of its three resonance structures.

Because of this resonance, the molecule has bilateral symmetry across the plane of the shared carbon pair, as well as across the plane that bisects bonds C2-C3 and C6-C7, and across the plane of the carbon atoms. Thus there are two sets of equivalent hydrogen atoms: the alpha positions, numbered 1, 4, 5, and 8, and the beta positions, 2, 3, 6, and 7. Two isomers are then possible for mono-substituted naphthalenes, corresponding to substitution at an alpha or beta position. Bicyclo[6.2.0]decapentaene is a structural isomer with a fused 4–8 ring system.

Therefore four (4) double bonds will be added to give each carbon atom an octet structure.

8 0
2 years ago
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Nutka1998 [239]

Answer:

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Explanation:

First thing's first, let's ensure that all the reactions given are balanced. This is given as;

CO(g) + 1/2 O2(g )→ CO2(g)

Li(s) + 1/2 F2(l) → LiF(s)

C(s) + O2(g) → CO2(g)

CaCO3(g) → CaO + CO2(g)

2Li(s) + F2(g) → 2LiF(s)

For the condition to be valid;

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- The lements haveto be in their state at room temperature. Fluorine is a gas, not a liquid, at room temperature ans pressure, so 2 is not a correct answer.

This leaves us with reactions 1, 3 and 5 as the correct reactions that satisify the condition.

3 0
2 years ago
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