Explain why aldehydes and ketones have a higher boiling point than the corresponding hydrocarbons.
Explain why aldehydes and ketones have a higher boiling point than the corresponding hydrocarbons.
Question 8 1 pts Aldehydes and ketones would always have a higher boiling point than the corresponding hydrocarbon with the same number of carbon atoms. O False O True « Previous Next >
Why do alcohols and carboxylic acids have a higher boiling points than hydrocarbons and halocarbons?
1. True and False Question (0.5 point per question) a) Carbonyl compounds have higher boiling points than hydrocarbons, but lower boiling points than corresponding alcohols. b) Aldehydes and ketones react with primary amines to form imines and with secondary amines to form enamines. c) Aldehydes and ketones can be oxidized to carboxylic acids. d) Diols can form acetal with the ketone or aldehyde to protect them for selective reduction of the ester. e) The electron-withdrawing group in Wittig reagent does...
Explain why acetic acid has a higher boiling point than ethyl alcohol ?
Why does Isopropanol C3H8O have a higher boiling point at 82.5 degrees than Ethyl Acetate C4H8O2 (a larger molecule) which has a Boiling point of 77.1 degrees? Please explain with detail. Thank you
TION 5 the general reactivity trend seen below. Why are aldehydes more reactive than ketones with respect to carbonyl addition General reactivity: formaldehyde > aldehydes > ketones T - 3 (12pt) T Arial
why does HCN have a higher boiling point than FCN? ( has to do with intermolecular forces?)
based on the difference in structures, why does ethyl butyrate have a higher boiling point than 2-butanone?
True and False questions!! 1. True and False Question (1) Carbonyl compounds have higher boiling points than hydrocarbons, but lower boiling points than corresponding alcohols. (2) Aldehydes and ketones react with primary amines to form imines and with secondary amines to form enamines. (3) Aldehydes and ketones can be oxidized to carboxylic acids. (4) Diols can form acetal with the ketone or aldehyde to protect them for selective reduction of the ester (5) The electron-withdrawing group in Wittig reagent does...
Q3. Explain why the reaction of aldehydes & ketones is. nucleophilic addition. Use pka values in your explanation- (not nucleophilic substution.