why enol is unstable?
Why it tend to be unstable and isomerize to the keton form?
why enol is unstable? Why it tend to be unstable and isomerize to the keton form?
Draw the mechanism for the conversion of propanedial in its keto form to its enol form under basic and acidic conditions. Do the same for the conversion from the enol form to the keto form.
Societies with skewed sex ratios tend to be unstable. Please use current U.S. Census to provide sex ratio in the United States, sex ratio in New Jersey and in Los Angeles. How do you predict population change and interracial relationship in future? Why?
Use the electron configurations of the alkali metals to explain why they tend to form 1+ ions.
In keto-enol tautomerization, steric repulsions can be larger for the keto form than the enol configuration. This effect is thought to be less important in the β-ketoesters, in which the R to R separation is greater. Discuss the above statements.
Use the electron configurations of the alkali metals to explain why they tend to form 1+ ions.
What is the most stable enol form of 1,3-cyclohexanedione?
4. Which tautomer of phenol is favored and why? A. enol, better hydrogen bonding C. keto, better CO resonance B. enol, aromaticity D. 1:1 both keto and enol forms are favored 5. Which base will completely and irreversibly form the enolate of the compound shown?: ? A. KOH B. NaOH C. NHS D. NaNH2
An explanation as to why S atoms tend to form single S-S bonds rather than the double bonds observed in O2.
Draw a structural formula for the enol form of the carbonyl compound below.
Which of the following is the most stable enol form of 1,3-cyclohexanedione?