I'm a beginner in the subject. It's a category that is overviewed in my AP Chem class. I need some help understanding the following:

dimethyl-n-butylmethane
diethylmethylmethane
diethyldimethylmethane
trimethylisobutylmethane
diethylisopropylmethane
dimethylisopropylmethane

...to be continued.

Basically, I understand the ethyl, methyl, butyl, and methane compounds on their own, but I don't know how to contruct them. From there, I might be able to find each isomer and use the IUPAC nomenclature to name them. We were introduced to the subject in class, given homework, and just sort of expected to do it. I'm very lost, and starting to doubt my understanding of chemistry.

Help?

I'm not sure this will address your trouble because I'm a little confused by the question. However, for a beginner, here are the basics.

Carbon has a valence of 4; therefore, there will ALWAYS be four bonds attached somehow and someway. We can't draw diagrams on these boards but I can try to explain a couple of them.
For diethylmethylmethane do the following:
Draw a methane molecule.
&nbsp&nbspH
&nbsp&nbsp|
H-C-H
&nbsp&nbsp|
&nbsp&nbspH
(I hope that comes out well enough but of course you know how to draw methane, anyway.)
Now, remove one of the H atoms and replace it with a -CH3 group. Then remove another of the H atoms from the original CH4 structure and replace it with -C2H5 group. Do the same with another of the original H atoms. That gives you a central C with 1 H attached, two C2H5 groups attached, and a CH3 group attached.
I hope this helps but don't hesitate to let me know if this isn't what you were looking for.

The structure didn't come out quite right. Here is another go at it.

&nbsp H
&nbsp |
H-C-H
&nbsp |
&nbsp H

A little better. You get the idea.

Of course! I'd be happy to help you understand how to construct and name these compounds. The compounds you mentioned are known as alkanes, which are a type of hydrocarbon consisting of only carbon and hydrogen atoms. Alkanes have a general formula of CnH2n+2, where "n" represents the number of carbon atoms.

To construct these compounds, you need to understand how to combine different alkyl groups (methyl, ethyl, butyl) with a parent hydrocarbon chain (such as methane, ethane, or butane). Here's a step-by-step guide:

1. Start by identifying the parent hydrocarbon chain. The parent chain is the longest continuous sequence of carbon atoms in the molecule. In your examples, the parent chains are methane (1 carbon), ethane (2 carbons), and butane (4 carbons).

2. Next, identify the substituent groups (alkyl groups) attached to the parent chain. In your examples, the substituents are methyl, ethyl, and butyl.

3. Determine the position of the substituents. Number the carbon atoms in the parent chain, starting with the end nearest to a substituent group. If there are multiple substituents, you'll need to assign numbers to each one. For example, in "diethylmethylmethane," the methyl group would be located on the second carbon atom of the parent chain, and the two ethyl groups would be attached to separate carbon atoms.

4. Combine the substituents with the parent chain to form the compound. Use hyphens to separate the substituents and the parent chain. For example, "diethylmethylmethane" would be constructed by combining two ethyl groups with a methyl group on the second carbon of the parent chain.

Once you have constructed the compounds, you can use IUPAC nomenclature rules to name them properly. The IUPAC rules provide a systematic method for naming organic compounds. Remember to identify the substituents, assign numbers to the substituents, and use appropriate prefixes (di-, tri-, tetra-) to indicate multiple instances of the same substituent.

I hope this explanation helps you understand how to construct and name these compounds! If you have any more questions, feel free to ask.