|Molar mass||86.178 g·mol−1|
How do you write 3-Methylpentane?
3-Methylpentane is a branched-chain alkane with the molecular formula C6H14. It is a structural isomer of hexane composed of a methyl group bonded to the third carbon atom in a pentane chain.
How many Stereocenters are in 3-Methylpentane?
|Property Name||Property Value||Reference|
|Defined Bond Stereocenter Count||Computed by PubChem|
|Undefined Bond Stereocenter Count||Computed by PubChem|
|Covalently-Bonded Unit Count||1||Computed by PubChem|
|Compound Is Canonicalized||Yes||Computed by PubChem (release 2021.05.07)|
Is 3 Methylpentane an asymmetric carbon?
3-Methylhexane is a branched hydrocarbon with two enantiomers. It is one of the isomers of heptane. The molecule is chiral, and is one of the two isomers of heptane to have this property.
Is 3-methylhexane R or S?
3-Methylhexane is a branched hydrocarbon with two enantiomers. It is one of the isomers of heptane. The molecule is chiral, and is one of the two isomers of heptane to have this property. The enantiomers are (R)-3-methylhexane and (S)-3-methylhexane.
Are 2-methylpentane and 3 Methylpentane position isomers?
2-Methylpentane is an alkane. Methyl pentane appears as colorless liquid. Isomers (2-methyl, 3-methyl) are possible and present in technical mixtures or singly for research purposes.
Is 3 Methylpentane optically active?
3- Methylhexane C2H5−C∗H(CH3)−C3H7 is optically active because of molecular unsymmetry and chiral carbon. Hence it is capable of existing as a pair of enantiomers.
Is 2-Methylpentane saturated?
Explanation: The formula of 2-methylpentane≡C6H14 … … 2-methylpentane is thus a saturated molecule, with NEITHER double bonds, NOR ring junctions…