Mesoporous material synthesized using ultrafine coal fly ash as a source for silicon and aluminium with cetyl trimethyl ammonium bromide as the structure directing agent has been found to be a good support for enhancing the stereoselectivity of reduction of some substituted cyclohexanones. Exclusive formation of trans-4-t-butyl cyclohexanol and 4-methyl cyclohexanol is evidenced by the appearance of single peaks in 1HNMR spectra ( = 3.5), which are due to axial CH protons. In other cases, enhancement of stereoselectivity has been observed. Apparently, Lewis/Bronsted acid sites present in the mesoporous material activate such preference for the formation of isomers with an equatorially disposed OH group. A probable transition state has been suggested.