There are many possibilities depending on the saturation. A few possible options are listed here.
butane
2-methyl-propane
cyclobutane
methylcyclopropane
1-butene
2-butene
2-methyl-prop-1-ene
1,2-butadiene
1,3-butadiene
1-butyne
2-butyne
The balanced equation for the complete combustion of cyclooctane (C8H16) is: C8H16 + 12O2 -> 8CO2 + 8H2O
C8H16 is a covalent compound. It consists of carbon and hydrogen atoms bonded together through sharing of electrons, which is characteristic of covalent compounds.
The IUPAC name for the hydrocarbon C14H30 is tetradecane. It is a straight-chain alkane with 14 carbon atoms.
The IUPAC name for the cyclic hydrocarbon compound commonly known as cyclohexane is "cyclohexane."
C8H16 does not specify the arrangement of atoms, so it is neither cis nor trans. The cis/trans notation is used to describe relative positions of substituents on a molecule, typically alkenes or cycloalkanes.
c7 is heptacarbon i dont know what h16 is that is what i am trying to figure out
C8H16 + Br2 -> C8H16Br2
The balanced equation for the complete combustion of cyclooctane (C8H16) is: C8H16 + 12O2 -> 8CO2 + 8H2O
What is the substance? A hydrocarbon? An alkane? hydrocarbon empirical formula = CH2 so X = 16 --- C8H16 for alkanes the rule is 2n + 2 so X = 18 --- C8H18 or, could be other forms, so message me if further help needed
This equation, for complete combustion, is C8H16 + 12 O2 => 8 CO2 + 8 H2O. (The first formula in the equation is a molecular formula for ethylcyclohexane.)
C8H16 is a covalent compound. It consists of carbon and hydrogen atoms bonded together through sharing of electrons, which is characteristic of covalent compounds.
HC
The IUPAC name for the hydrocarbon C14H30 is tetradecane. It is a straight-chain alkane with 14 carbon atoms.
Alkanes are saturated, so if the hydrocarbon has -ane at the end of it, it is saturated.
1,2 diflouroethene
The IUPAC name for the cyclic hydrocarbon compound commonly known as cyclohexane is "cyclohexane."
C8H16 does not specify the arrangement of atoms, so it is neither cis nor trans. The cis/trans notation is used to describe relative positions of substituents on a molecule, typically alkenes or cycloalkanes.