Skip to main content

2-Methylhex-2-ene

ADVERTISEMENT
Identification
Molecular formula
C7H14
CAS number
623-37-0
IUPAC name
2-methylhex-2-ene
State
State

At room temperature, 2-Methylhex-2-ene exists as a liquid.

Melting point (Celsius)
-124.00
Melting point (Kelvin)
149.15
Boiling point (Celsius)
93.70
Boiling point (Kelvin)
366.85
General information
Molecular weight
98.19g/mol
Molar mass
98.1920g/mol
Density
0.7183g/cm3
Appearence

2-Methylhex-2-ene is a colorless liquid with a characteristic aliphatic odor. It is typically clear and may have a slightly oily texture.

Comment on solubility

Solubility of 2-methylhex-2-ene

2-methylhex-2-ene, with its chemical formula C7H14, is an alkenic organic compound known for its unsaturation. When discussing its solubility, it's essential to note the following key points:

  • Non-polar Nature: Being a hydrocarbon, 2-methylhex-2-ene is largely non-polar, which limits its solubility in polar solvents.
  • Solubility in Organic Solvents: It is soluble in non-polar organic solvents like hexane, benzene, and other similar hydrocarbons.
  • Poor Solubility in Water: Due to its hydrophobic characteristics, 2-methylhex-2-ene is almost insoluble in water, making it more compatible with oily or lipid phases.

The solubility of this compound can significantly influence its behavior in various chemical processes, especially in organic synthesis and reaction mechanisms. As a rule of thumb, “like dissolves like” applies perfectly here; thus, understanding its solubility in different mediums is crucial for practical applications.

Interesting facts

Interesting Facts about 2-Methylhex-2-ene

2-Methylhex-2-ene is an intriguing organic compound belonging to the class of alkenes, which are known for their carbon-carbon double bonds. This particular compound exhibits several fascinating characteristics and applications that make it notable in the realm of chemistry.

Key Features

  • Structural Importance: The presence of the double bond in 2-methylhex-2-ene is essential for its reactivity and properties. The molecular structure allows for its use in various chemical reactions, such as hydrogenation, polymerization, and hydroformylation.
  • Synthesis: 2-Methylhex-2-ene can be synthesized through different methods, mainly via dehydration of the corresponding alcohol, making it an important intermediate in organic synthesis.
  • Applications: It serves as a building block for the creation of more complex organic molecules. Its derivatives are often utilized in the production of perfumes, plastics, and as solvents.
  • Isomeric Nature: Being an alkene, it can exhibit geometric isomerism due to the presence of the double bond, leading to different configurations that can have varying physical and chemical properties.

Chemical Behavior

As an alkene, 2-methylhex-2-ene reacts with various reagents to form different products. For example, it can undergo:

  • Addition Reactions: Such as electrophilic addition, where halogens or hydrogen add across the double bond.
  • Oxidation Reactions: That can convert the double bond into alcohols or ketones, widening its applicability in organic synthesis.

In Summary

2-Methylhex-2-ene is more than just a simple alkene; it is a compound with a range of functionalities and potential applications in chemical industries. As students and scientists explore its reactivity, they unlock numerous opportunities for innovative chemical transformations. The study of such compounds not only enriches our understanding of organic chemistry but also bridges the gap between theory and practical applications.

Synonyms
2-METHYL-2-HEXENE
2-Hexene, 2-methyl-
C3H7CH=C(CH3)2
DTXSID70181810
NSC 73928
DTXCID10104301
678-601-8
bwekdyghdchwen-uhfffaoysa-n
inchi=1/c7h14/c1-4-5-6-7(2)3/h6h,4-5h2,1-3h
2738-19-4
2-methylhex-2-ene
NSC73928
MFCD00027232
NSC-73928
AKOS024429364
M0526
T72209