I have to answer the following questions about C3H7Cl:

Are there different constitutional isomers for this formula, are there different cis/trans isomer, and are there different conformers?

I know that C3H7Cl can be drawn two ways:

H-C-C-C-Cl With H's above and below the 3 carbons

H-C-C-C-H with H's above and below the carbons and a Cl on one of the carbons.

I am not sure if these two ways would be considered conformers or constitutional isomers?

To determine whether the two ways you have drawn C3H7Cl represent conformers or constitutional isomers, let's first define what each term means in the context of organic chemistry:

1. Constitutional isomers: Constitutional isomers are different compounds that have the same molecular formula but differ in the connectivity of atoms. In other words, they have different arrangements of atoms.

2. Conformers: Conformers are different spatial arrangements of the same molecule achieved by rotation around single bonds.

Now, let's analyze the two ways you have drawn C3H7Cl:

1. H-C-C-C-Cl with H's above and below the 3 carbons.
2. H-C-C-C-H with H's above and below the carbons and a Cl on one of the carbons.

Based on this information, here's how we can determine whether they are conformers or constitutional isomers:

Constitutional isomers: To determine if the two structures are constitutional isomers, we need to check if they have the same molecular formula and differ in connectivity. In this case, both structures have the same molecular formula (C3H7Cl), but they differ in connectivity (the position of the chlorine atom), so they can be considered constitutional isomers.

Conformers: Conformers are different spatial arrangements of the same molecule achieved by rotation around single bonds. In this case, the two structures you have drawn can be considered conformers because they can interconvert simply by rotating around the carbon-carbon (C-C) bond axis.

In summary, the two ways you have drawn C3H7Cl are constitutional isomers because they have the same molecular formula but differ in connectivity. They can also be considered conformers since they can interconvert by rotation around the C-C bond axis.