4-methylcyclohexene, 3-methylcyclohexene and 1-methylcyclohexene which is the major product because it is trisubstituted as opposed to the first two which are only disubstituted
The dehydration of 4-methylcyclohexanol yields only one product, 4-methylcyclohexene. --Ron Actually, at least three different isomers of methyl cyclohexene are produced. 1 methyl cyclohexene, 3-methyl cyclohexene and 4-methyl cyclohexene. It is a fascinating reaction undergoing a lot of recent study. It is becoming the classic example of the "Evelyn Effect" wherin the proportions of different products of a reaction vary with time as a result of the fact that the rates of the processes generating the different products differ in themselves. See http://ochemonline.pbwiki.com/f/Dehydration_Blog.doc for more information. - GM
A dehydration reaction involves the loss of a water molecule. The products that would be obtained from the dehydration of 2-methyl 1-1-cyclohexanol are 1-methylcyclohexene and 3-methylcyclohexene.
4-methylcyclohexene, 3-methylcyclohexene and 1-methylcyclohexene which is the major product because it is trisubstituted as opposed to the first two which are only disubstituted
2Methyl-1-propanol is isobutanol...I dont know for what purpose you want to replace this with isoproponol.
Hexane is a 6 carbon chain. starting at one end, number the carbons 1 - 6. 2-methyl 3-chloro means that the methyl group attaches to carbon 2, and the chlorine attaches to carbon 3. 3-methyl 2-chloro would simply be the other way around. They are two unique and different compounds.
According to the label it's 2-hydroxy-2methyl-1-phenyl-1-propanone and 1,6-hexanediol diacrylate. The hydroxy propanone acts as a photo-initiator that causes the diacrylate to polymerize.