What is the major product of the dehydration of 2-methylcyclohexanol?
1- methylcyclohexene
Conclusions: It is evident that the dehydration of 2-methylcyclohexanol in H3PO4 gave 1- methylcyclohexene as the major product, as predicted by Saytzev (more substituted C=C being more stable).
What would be the major product obtained from the e1 dehydration of 2-methylcyclohexanol?
Conclusions: It is evident that the dehydration of 2-methylcyclohexanol in H3PO4 gave 1- methylcyclohexene as the major product, as predicted by Saytzev (more substituted C=C being more stable).
What is the final step in the mechanism of the dehydration of 2-methylcyclohexanol?
Furthermore, the greater stability of the tertiary carbocation over the secondary cation makes the final step of the reaction thermodynamically somewhat reversible, so that if the reaction is carried out over longer times, a relatively larger fraction of methylenecyclohexane (compared to 1-methylcyclohexene) is …
What is the density of 2-methylcyclohexanol?
0.93 g/mL
0.93 g/mL at 25 °C (lit.)
How does 2-methylcyclohexanol react with alkali metals?
2-METHYLCYCLOHEXANOL is an alcohol. Flammable and/or toxic gases are generated by the combination of these materials with alkali metals, nitrides, and strong reducing agents. Contact with strong oxidizers may cause fires and explosions. They react with oxoacids and carboxylic acids to form esters plus water.
Which is the chemical formula for 2-methylcyclohexanol?
2-Methylcyclohexanol PubChem CID 11418 Structure Find Similar Structures Chemical Safety Laboratory Chemical Safety Summary (LCSS Molecular Formula C7H14O Synonyms 2-METHYLCYCLOHEXANOL 583-59-5 Cyclohexan
How is 2-methylcyclohexanol dehydrated to form cyclic alkenes?
The acid-catalyzed dehydration of 2-methylcyclohexanol to form a mixture of cyclic alkenes has become a standard experiment in the organic chemistry and upper-level laboratory curricula at several colleges and universities (1-4). Among other things, it illustrates the utility of Zaitsev’s rule.
Why is the regioselectivity of 2-methylcyclohexanol found through GC?
The use of simple distillation did not give the reaction enough time to produce the second, less likely minor product. After the distillation, the regioselectivity of the compound was found through GC.