I can only think of 14 of them, but i know there are a few more 1-chlorohexane 2-chlorohexane 3-chlorohexane 1-chloro-2-methylpentane 1-chloro-3-methylpentane 1-chloro-4-methylpentane 2-chloro-3-methylpentane 2-chloro-4-methylpentane 3-chloro-2-methylpentane 1-chloro-2,2-dimethylbutane 3-chloro-2,2-dimethylbutane 1-chloro-3,3-dimethylbutane 1-chloro-2,3-dimethylbutane 2-chloro-2,3-dimethylbutane
Hexane has five total Isomers: - Hexane is a straight chain of six carbon atoms:
CH3CH2CH2CH2CH2CH3 - 2-Methylpentane, also called Isohexane, has a five carbon chain with one methyl branch on the second group:
-CH3CH(CH3)CH2CH2CH3 -3-Methylpentane has a five Carbon chain with a Methyl branch on the Third group:
-CH3CH2CH(CH3)CH2CH3 -2/3-Dimethylbutane has a four carbon chain with one Methyl branch on the both the Second and Third branch:
-CH3CH(CH3)CH(CH3)CH3 -2/2-Dimethylbutane, also called Neohexane, has a four carbon chain with two Methyl groups on the Second branch:
-CH3C(CH3)2CH2CH3
2-methyl hexane ; 3-methyl hexane ; 2,3-dimethyl pentane ; 2,4-dimethyl pentane ; 2,2,3-trimethyl butane...
The nine isomers of heptane are:
n-heptane (or normal heptane)
2-methylhexane
3-methylhexane
2,2-dimethylpentane
2,3-dimethylpentane
2,4-dimethylpentane
3,3-dimethylpentane
3-ethylpentane
And 2,2,3-trimethylbutane
There are a total of 16 possible isomers of a D-ketohexofuranose. This includes aldohexose isomers as well as ketohexose isomers. The structural diversity arises from variations in the arrangement of hydroxyl (-OH) groups and the position of the carbonyl group.
The possible isomers of C3H8O are propane-1-ol, propane-2-ol, and methoxypropane.
There are four possible functional isomers for tetrose sugars. They include erythrose, threose, erythrulose, and threulose. Each of these isomers has a unique arrangement of functional groups that determine its chemical properties and biological functions.
For a molecule with n chiral centers, there are a possible 2^n isomers that can be formed.
It depends on which of the 24 isomers of octane you are after.
Possible position isomers of C6H13Cl include 1-chlorohexane, 2-chlorohexane, 3-chlorohexane, 4-chlorohexane, 5-chlorohexane, and 6-chlorohexane. These isomers have the same molecular formula but differ in the position of the chlorine atom along the carbon chain.
Three isomers of C2HfClBr are possible.
Diacetylferrocene can have three possible isomers: symmetrical cis-diacetylferrocene, symmetrical trans-diacetylferrocene, and unsymmetrical diacetylferrocene.
There are a total of 16 possible isomers of a D-ketohexofuranose. This includes aldohexose isomers as well as ketohexose isomers. The structural diversity arises from variations in the arrangement of hydroxyl (-OH) groups and the position of the carbonyl group.
There are three cyclic isomers possible for the formula C3H6O: two variations of oxirane and one of cyclopropanol. There are two acyclic isomers: propanal and 2-propanol.
Three other positional isomers are possible,, 1,2 - 1,3 and 1,4 bromochloro isomers.
The possible isomers of C3H8O are propane-1-ol, propane-2-ol, and methoxypropane.
Cis and trans isomers are possible due to restricted rotation around a double bond. In cis isomers, the functional groups are on the same side of the molecule, while in trans isomers, they are on opposite sides. This difference in spatial arrangement leads to different physical and chemical properties between the two isomers.
There are four possible functional isomers for tetrose sugars. They include erythrose, threose, erythrulose, and threulose. Each of these isomers has a unique arrangement of functional groups that determine its chemical properties and biological functions.
There are two types of geometric isomers possible in octahedral complex ions: cis and trans isomers. For a complex with six different ligands, there can be a maximum of 30 different cis and trans isomers.
4
The isomers of C5H11Cl include n-pentyl chloride, isopentyl chloride (or 2-methylbutyl chloride), and neopentyl chloride (or 2,2-dimethylpropyl chloride).