In this video, we're going to talk about the way of naming cycloalkanes. Now we're going to state the rules for naming cyclic alkanes or cycloalkanes, which are very similar to naming alkanes with substituents. Here, our naming convention will focus on the location of each substituent and, because it's a cyclic alkane or cycloalkane, the parent chain is named as a cyclo parent chain. So now that we know the basic naming structure, let's move on to the next video where we start naming different types of cycloalkane compounds.
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Naming Cyclic Alkanes - Online Tutor, Practice Problems & Exam Prep
Naming cycloalkanes follows similar rules to naming alkanes with substituents. The parent chain is designated as a cyclo compound, and the position of each substituent is crucial for accurate naming. Understanding these conventions is essential for identifying and classifying cyclic hydrocarbons, which are important in organic chemistry. Mastery of this naming system aids in recognizing structural isomers and their properties, enhancing comprehension of chemical reactions involving cycloalkanes.
Rules for Naming Cyclic Alkanes Concept 1
Video transcript
Naming Cyclic Alkanes Example 1
Video transcript
Now here in this example question it says, determine the systematic name of the following alkane. So to do that, we're going to employ the following steps. So, step 1, it says, assign a name to the alkane ring. The ring here will serve as the parent, according to its prefixes. Now, you're going to add the prefix 'cyclo,' to the name of the alkane ring, because it's no longer just an alkane, it's a cyclic alkane. So we're going to use 'cyclo.' Now, step 2, you're going to assign names to all the substituents on that ring. Step 3, start numbering the chain from the closest substituent. Now, if there is only one substituent, the location is not necessary. If tied between substituents, compare the next closest substituent; if it's still a tie, number in alphabetical order. From our previous videos in terms of naming alkanes with substituents, we'd use steps 4 to 6. So repeating the same steps from that previous topic. Remember, this has to do with giving a location for the substituents, it has to do with naming substituents alphabetically, and then remember that we use commas to separate numbers from one another, and we use dashes to separate letters and numbers from one another. Now if we take a look here, we have a ring with 1, 2, 3, 4, 5, 6 carbons long in terms of our cyclic alkane. 6 carbons for an alkane is hexane, but it's not just hexane, it's a cyclic hexane. So we use the prefix cyclo. So this is a cyclohexane ring, and attached to it is a 3 carbon alkyl group. Since the bond is at one of the ends of this 3 carbon alkyl group, it represents propyl. Now here, there's only this one substituent, so you don't need to give its numerical location. Because wherever it is located, that's where carbon number 1 will be in this case. So here, we'd say that this is called propylcyclohexane. This will be the name of this particular cyclic alkane with its substituent.
Give a systematic name for the below compound.
1-sec-butyl-3-methylcyclopentane
1-methyl-3-sec-butylcyclopentane
1-butyl-3-methylcyclopentane
1-methyl-3-butylpentane
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Here’s what students ask on this topic:
What are the rules for naming cycloalkanes?
Naming cycloalkanes follows specific rules similar to naming alkanes with substituents. The parent chain is named as a 'cyclo' compound, indicating its cyclic nature. The steps include: 1) Identify the longest continuous carbon chain in the ring. 2) Number the carbon atoms in the ring starting from the carbon with the substituent that comes first alphabetically. 3) Assign numbers to substituents to give the lowest possible numbers. 4) List substituents in alphabetical order, using prefixes like di-, tri-, etc., if necessary. For example, 1,2-dimethylcyclohexane indicates two methyl groups on the first and second carbons of a cyclohexane ring.
How do you determine the parent chain in cycloalkanes?
In cycloalkanes, the parent chain is the ring itself, regardless of the number of carbons in any substituent chains. The ring is named as a 'cyclo' compound, such as cyclopentane for a five-carbon ring or cyclohexane for a six-carbon ring. The longest continuous carbon chain within the ring is considered the parent chain. If there are substituents, the ring is still the parent chain, and the substituents are named and numbered accordingly.
How do you number substituents in cycloalkanes?
To number substituents in cycloalkanes, start by numbering the carbon atoms in the ring. Begin with the carbon that has the substituent which comes first alphabetically. Continue numbering in a direction that gives the substituents the lowest possible numbers. For example, in 1-ethyl-2-methylcyclopentane, the ethyl group is on carbon 1 and the methyl group is on carbon 2, ensuring the lowest possible numbering for the substituents.
What is the difference between naming alkanes and cycloalkanes?
The primary difference between naming alkanes and cycloalkanes is the inclusion of the 'cyclo' prefix in cycloalkanes to indicate a ring structure. In alkanes, the longest continuous carbon chain is identified and named, while in cycloalkanes, the ring itself is the parent chain. Additionally, the numbering of substituents in cycloalkanes starts from the carbon with the substituent that comes first alphabetically, ensuring the lowest possible numbers for all substituents.
Why is it important to understand the naming conventions of cycloalkanes?
Understanding the naming conventions of cycloalkanes is crucial for accurately identifying and classifying cyclic hydrocarbons in organic chemistry. Mastery of this system aids in recognizing structural isomers and their properties, which is essential for predicting and understanding chemical reactions involving cycloalkanes. Proper naming ensures clear communication among chemists and helps in the study and application of these compounds in various chemical contexts.
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- What are the IUPAC names of the following cycloalkanes? Remember to assign priority to the attached groups alp...
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- Consider the compound ethylcyclopentane. (7.4, 7.7, 8.6, 11.3, 11.4)a. Draw the line-angle formula for ethylcy...
- Draw the line-angle formula for each of the following:b. ethylcyclopentane
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- Draw the line-angle formula for each of the following:d. 2,3-dichlorohexane
- Draw the condensed structural or line-angle formula if cyclic, for each of the following: (11.3, 11.5, 11.6)a....
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