C. If the banks of the river are eroding, then the river will be wider.
Answer:
Sorry
Explanation:
Sorry this is not chemistry but I always try to answer but this time I can't I am so so sorry
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.
You need to find which intermolecular forces are between the molecules
dipole-dipole,h bonds, etc.
I'm not very good at explaining but this is what my prof said to help us
Identify the class of the molecule or molecules you are given. Are they nonpolar species, ions or
do they have permanent dipoles? Is there only one species or are there two?
In the case of ONE species (i.e., a pure substance), the intermolecular forces will be between
molecules of the same type. So if you are dealing with ions, the intermolecular forces will be ION-
ION or IONIC. If you are dealing with dipoles, then the intermolecular forces will be DIPOLE-
DIPOLE. If you are dealing with nonpolar species, the intermolecular forces will be DISPERSION
or VAN DER WAALS or INDUCED DIPOLE-INDUCED DIPOLE (the last three are desciptions
of the same interaction; regrettably we cannot call them nonpolar-nonpolar!).
In the case of TWO species (i.e., a mixture), the intermolecular forces will be between molecules of
one type with molecules of the second type. For example, ION-DIPOLE interactions exist between
ions dissolved in a dipolar fluid such as water.
Answer:
C) Temperature and Kinetic Energy.
Explanation:
Hello there!
In this case, according to the generic heating curve on the attached file, it possible to see that on the point C, whereas the line is diagonal, the temperature increases, but also the kinetic energy increases because the molecules gain energy due to the increase of the temperature. It is important to say that on flat lines, like those on B and D, the phase change takes place and just the potential energy change.
In such a way, we infer that the answer is C) Temperature and Kinetic Energy.
Best regards!