Answer:
A)
1. Reaction will shift rightwards towards the products.
2. It will turn green.
3. The solution will be cooler..
B) It will turn green.
Explanation:
Hello,
In this case, for the stated equilibrium:
In such a way, by thinking out the Le Chatelier's principle, we can answer to each question:
A)
1. If potassium bromide, which adds bromide ions, is added more reactant is being added to the solution, therefore, the reaction will shift rightwards towards the products.
2. The formation of the green complex is favored, therefore, it will turn green.
3. The solution will be cooler as heat is converted into "cold" in order to reestablish equilibrium.
B) In this case, as the heat is a reactant, if more heat is added, more products will be formed, which implies that it will turn green.
Regards.
Answer:
See explanation below
Explanation:
The question is incomplete, cause you are not providing the structure. However, I found the question and it's attached in picture 1.
Now, according to this reaction and the product given, we can see that we have sustitution reaction. In the absence of sodium methoxide, the reaction it's no longer in basic medium, so the sustitution reaction that it's promoted here it's not an Sn2 reaction as part a), but instead a Sn1 reaction, and in this we can have the presence of carbocation. What happen here then?, well, the bromine leaves the molecule leaving a secondary carbocation there, but the neighbour carbon (The one in the cycle) has a more stable carbocation, so one atom of hydrogen from that carbon migrates to the carbon with the carbocation to stabilize that carbon, and the result is a tertiary carbocation. When this happens, the methanol can easily go there and form the product.
For question 6a, as it was stated before, the mechanism in that reaction is a Sn2, however, we can have conditions for an E2 reaction and form an alkene. This can be done, cause the extoxide can substract the atoms of hydrogens from either the carbon of the cycle or the terminal methyl of the molecule and will form two different products of elimination. The product formed in greater quantities will be the one where the negative charge is more stable, in this case, in the primary carbon of the methyl it's more stable there, so product 1 will be formed more (See picture 2)
For question 6b, same principle of 6a, when the hydrogen migrates to the 2nd carbocation to form a tertiary carbocation the methanol will promove an E1 reaction with the vecinal carbons and form two eliminations products. See picture 2 for mechanism of reaction.
A - Sulfur dioxide is an ion because it contains 2 or more elements, and it is a solid
Answer:
2x+3y=-6
4x+3y=12
3x-y=5
5x+3y=1
Explanation:
standard form: ax + by = C
<span>To solve this problem, You need to look up a picture/diagram of the electromagnetic spectrum. This will have the wave regions listed as well</span> as frequencies and wavelength.
Wavelength is distance/length of one wave, which can be calculated using frequency (hz = s^-1) and the speed of light.
2.998 x 10^8 m/s ÷ 3 x 10^19 s^-1 = 9.99 x 10^-12 m
The Frequency given falls in between X-rays and Gamma rays. The wavelength however; is in the Gama ray region.
