Ask a New Question

Question

Consider the compounds 4-tert-butylcyclohexanol and 4-tert-butylcyclohexanone. Using silica gel plates, which of the two compounds will have the higher Rf value when ethyl acetate is the developing solvent? Which will have the higher Rf value when dichloromethane is the developing solvent? Give reasoning for each case.

How do I go about figuring this out? Should I pay attention to the polarity of each compound?
9 years ago

Answers

Related Questions

Are any of the following a tertiary amine 2-methyl-2-butanamine N-Methyl-1-butanamine N-Methyl... Potassium tert-butoxide is a common base for E2 reactions because it is _______. A. weak base B.... 1if you open the tert-butyl chloride and tert-butyl bromide to the air for few hours? What happened... Why was the tert. butyl chloride finally washed with water? Why is tert. butyl chloride being washed with aqueous sodium hydrogen carbonate Consider compounds trans-4-tert-butylcyclohexanol and 4-tert-butylcyclohexanone below. Using silica... Why was the tert butyl chloride washed with aqueous sodium hydrogen carbonate? what gas was evolved... Where do the secondary and tertiary neurons synapse? Medulla oblongata Thoracic region of the... What is MCMV TERT AND FST
Ask a New Question
Archives Contact Us Privacy Policy Terms of Use