Identifying Cyclic Alkanes: C6H12 - C9H18 - C10H20

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In summary, the cyclic alkanes in the given image are named as follows: a. Butane - ethylcyclobutane (C6H12)b. Pentane - 1-methyl-3-propylcyclopentane (C9H18)c. Hexane - 2-ethyl-1,3-dimethylcyclohexane (C10H20).
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Homework Statement


Name each of the following cyclic alkanes, and indicate the formula of the compound.
http://img230.imageshack.us/img230/1042/organicnaming.jpg


Homework Equations





The Attempt at a Solution


a. The rectangle has four corners so four carbon for butane. The branch off has two carbons so eth-. Numbering the branch C as 1, the naming is 1-ethylcyclobutane with C6H12 because each corner is 1 C plus the C written and the H comes from subtracting 4 with the number of bonds connected to each of the C. Is this correct?

b. The pentagon has five corners so five corner for pentane. The branch off is prop- and meth-. Naming starts with alphabetical order so meth- first so the prop- is three. 1-methyl-3-propylcyclopentane. Logic from a., C9H18. Is this correct?

c. Hexane from six corners. Dimethyl and ethyl here. Is this named 1-ethyl-2,6-dimethylcyclohexane or 2-ethyl-1,3-dimethylcyclohexane? C10H20.

If there is a mistake, which part?
 
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312213 said:

Homework Statement


Name each of the following cyclic alkanes, and indicate the formula of the compound.
http://img230.imageshack.us/img230/1042/organicnaming.jpg


Homework Equations





The Attempt at a Solution


a. The rectangle has four corners so four carbon for butane. The branch off has two carbons so eth-. Numbering the branch C as 1, the naming is 1-ethylcyclobutane with C6H12 because each corner is 1 C plus the C written and the H comes from subtracting 4 with the number of bonds connected to each of the C. Is this correct?

b. The pentagon has five corners so five corner for pentane. The branch off is prop- and meth-. Naming starts with alphabetical order so meth- first so the prop- is three. 1-methyl-3-propylcyclopentane. Logic from a., C9H18. Is this correct?

c. Hexane from six corners. Dimethyl and ethyl here. Is this named 1-ethyl-2,6-dimethylcyclohexane or 2-ethyl-1,3-dimethylcyclohexane? C10H20.

If there is a mistake, which part?

A is just ethylcyclobutane. There is no need to number the substituent, since a cycloalkane with 1 substituent will always have it at the #1 carbon. You had the formula right.

B is correct.

C is 2-ethyl-1,3-dimethylcyclohexane (you number so as to give your substituents the lowest number possible, in the absence of priority substituents such as OH). Formula is correct.
 
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it is important to follow the IUPAC (International Union of Pure and Applied Chemistry) naming conventions for organic compounds. According to these conventions, the first step in naming a cyclic alkane is to identify the parent chain, which is the longest continuous chain of carbon atoms in the molecule. In all three compounds given, the parent chain is a ring of carbon atoms, so the suffix "-cyclo" is added to the name.

a. The first compound is correct. The parent chain is a four-carbon ring, so it is named cyclobutane. The branch off the ring is an ethyl group, so the full name is 1-ethylcyclobutane. The formula C6H12 is correct, as there are four carbons in the ring and two in the ethyl group, making a total of six carbon atoms.

b. The second compound is not named correctly. The parent chain is a five-carbon ring, so it is named cyclopentane. The branch off the ring is a methyl group and a propyl group, so the full name is 1-methyl-3-propylcyclopentane. The formula C9H18 is correct, as there are five carbons in the ring, one in the methyl group, and three in the propyl group, making a total of nine carbon atoms.

c. The third compound is also not named correctly. The parent chain is a six-carbon ring, so it is named cyclohexane. The branch off the ring is two methyl groups and one ethyl group, so the full name is 1,3-dimethyl-2-ethylcyclohexane. The formula C10H20 is correct, as there are six carbons in the ring, four in the methyl groups, and two in the ethyl group, making a total of ten carbon atoms.

In general, when naming cyclic alkanes, the parent chain is numbered starting from any side of the ring that allows the substituents (branches) to have the lowest possible numbers. In cases where there are multiple substituents, the substituents are named in alphabetical order and their positions are indicated by numbers. It is important to note that the prefixes "di-", "tri-", etc. are used to indicate multiple copies of the same substituent, while the prefixes "iso-" and "neo-" are used to indicate different
 

1. What is the general formula for cyclic alkanes?

The general formula for cyclic alkanes is CnH2n, where n represents the number of carbon atoms in the molecule. This means that for every carbon atom, there are two hydrogen atoms.

2. How do you identify a cyclic alkane?

Cyclic alkanes have a ring structure and do not contain any double or triple bonds. They also follow the general formula of CnH2n. To identify a specific cyclic alkane, you can use techniques such as gas chromatography or mass spectrometry.

3. What are some common examples of cyclic alkanes?

Some common examples of cyclic alkanes include cyclopropane (C3H6), cyclobutane (C4H8), cyclopentane (C5H10), and cyclohexane (C6H12). These molecules are commonly used in the production of various chemicals and materials.

4. How are cyclic alkanes different from straight-chain alkanes?

Cyclic alkanes have a ring structure, while straight-chain alkanes have a linear structure. This means that the carbon atoms in cyclic alkanes are bonded to each other in a ring, while in straight-chain alkanes, they are bonded in a straight line. Cyclic alkanes also tend to have higher boiling points and melting points compared to straight-chain alkanes.

5. What are the uses of cyclic alkanes?

Cyclic alkanes have various industrial uses, such as in the production of solvents, plastics, and fuels. They are also used in the manufacturing of pharmaceuticals and as additives in personal care products. Cyclic alkanes are also commonly used as refrigerants and propellants in aerosol products.

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