2-methylcyclohexanol---> 1-methylcyclohexene+ 3-methylcyclohexene + methylenecyclohexane
1-methylcyclohexene is the main product favored due to its more substituted double bond, followed by 3-methylcyclohexene and then methylenecyclohexane
it can lead to dehydration which can lead to low blood -pressure and slow heart beat
A molecule containing two double bonds would be an alkene. Alkenes have a carbon-carbon double bond in their structure.
The dehydration of 3-methyl 3-pentanol by heating would result in the formation of 3-methyl-2-pentene. The structural equation for this reaction would be: 3-methyl 3-pentanol → 3-methyl-2-pentene + H2O
Water is an inorganic substance that is always produced as a product of dehydration synthesis reactions. This process involves removing water molecules to form larger molecules.
Use bromine water (Br2) or acidified permanganate (H+/MnO4-) With permanganate: add the permanganate to the alkane and no reaction will occur, add the permanganate to the alkene and you will form a diol the solution will also turn from purple to colourless. With bromine water: add the bromine water to the alkane (plus you need sunlight) and you get a substitution reaction, this is a slow reaction. Add the bromine water to the alkene and you get an immediate addition reaction (this one does not need sunlight). When bromine water reacts with an alkene it is decolourised, the reddish brown bromine water turns from brown to colourless. This is because alkenes are unsaturated and contain a carbon to carbon double bond. If you did the bromine water test in a dark place say a cupboard then the alkene would decolourise but the alkane wouldn't because it needs UV/sunlight in order to react. in practice the cupboard is not necessary as the speed of decolourisation is so much faster with the alkene.
Cyclopentene would be produced from the dehydration of cyclopentanol.
The dehydration of tertiary alcohols typically leads to the formation of the most stable alkene. In the case of 2-methyl-2-butanol, the most stable alkene that would predominate as the product is 2-methyl-2-butene.
C5H10 can be both an alkane and an alkene. As an alkane, it would be pentane (C5H12), and as an alkene, it would be 1-pentene (C5H10). The presence or absence of a double bond in the molecule determines if it is an alkane or an alkene.
C4H8 can refer to either an alkene or an alkane. In the case of an alkene, it would be 1-butene, while for an alkane, it would be 2-methylpropene. The distinction can be made based on the presence of a double bond in the alkene.
The alkene will have 8 hydrogen atoms. It's chemical formula would be C4H8.
dehydration increases hematocrit
My guess would be dehydration and/or overheating.
it can lead to dehydration which can lead to low blood -pressure and slow heart beat
There would be none. In order for an alkene to have cis or trans isomers, there must be at least two identical groups or atoms attached to each of the two carbons of the double bond.
In an alkene, the carbon is sp2 hybridized (trigonal planar with 120° bond angles), while in an aromatic ring, the carbon is sp2 hybridized due to resonance. Therefore, a carbon in a molecule with both alkene and aromatic functional groups would also be sp2 hybridized.
Dehydration
dehydration