What is the structural formula for 3-Methylhexane?
PubChem CID | 7282 |
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Chemical Safety | Laboratory Chemical Safety Summary (LCSS) Datasheet |
Molecular Formula | C6H14 or CH3CH2CH(CH3)CH2CH3 |
Synonyms | 3-METHYLPENTANE 96-14-0 Pentane, 3-methyl- 3-Methyl-pentane UNII-XD8O3ML76T More… |
Molecular Weight | 86.18 |
Is 3-Methylhexane R or S?
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.
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CHEBI:143848 – 3-methylhexane.
ChEBI Name | 3-methylhexane |
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ChEBI ID | CHEBI:143848 |
Definition | An alkane that is hexane substituted by a methyl group at position 3. |
What type of functional group is attached to 3-Methylhexane?
What type of functional group is attached to 3-methylhexane? methyl group.
Is 3-Methylhexane chiral?
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.
What is the condensed formula for 2 Methylpentane?
2-Methylpentane
PubChem CID | 7892 |
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Chemical Safety | Laboratory Chemical Safety Summary (LCSS) Datasheet |
Molecular Formula | C6H14 or CH3CH(CH3)(CH2)2CH3 |
Synonyms | 2-METHYLPENTANE Isohexane 107-83-5 Pentane, 2-methyl- 2-Methylpentan More… |
Molecular Weight | 86.18 |
What is the structural formula of 3 Ethylpentane?
Condensed Structural Formula | Class of Alcohol | Common Name |
---|---|---|
CH 3CH 2OH | primary | ethyl alcohol |
CH 3CH 2CH 2OH | primary | propyl alcohol |
(CH 3) 2CHOH | secondary | isopropyl alcohol |
CH 3CH 2CH 2CH 2OH | primary | butyl alcohol |
What is the boiling point of 3 Methylhexane?
The given compound [3] Methyl hexane does not possess any symmetry element and also it has chiral carbon. Thus, [3] Methyl hexane is optically active.
Which of the following is the correct structural formula for 3 Methylcyclohexene?
3-Methylcyclohexene | C7H12 – PubChem.
Is 3/4 Dimethylhexane a meso compound?
3,4-diethylhexane has two asymmetric carbons,therefore it should have four enantiomers, however the enantiomers are reduced to three, because the 3(S),4(R) isomer is identical to the 3(R),4(S) isomer, since a plane of simmetry passes through the molecule between carbon 3 and 4.