please print and space out For the next two carbonyls are sites for addition but
ID: 1039932 • Letter: P
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please print and space out
For the next two carbonyls are sites for addition but carboxyls are sites for anone + methanol> Pentanoic acid+ methanol True-False Questions(25 marks) 1)Carboxylie acids are responsible for the sweet taste of fruits und vegetables 2) The boiling points of akohols are lower tham ketones of comparable molar mass. 3) As the alkyl part of an aildehyde gets larger they become less sol 4) Both aldehydes and ketones can undergo reduction reactions 5) Carboxylic acids with moee than five carbons are very water soluble. 6) The boiling points of carboxylic acids are lower than the cormesponding 7) Carboxylic acids with four or fewer carbons are very water soluble 8) When in solution, carboxylic acids are mostly in their ioniaed forms. 9) Aldehydes ubke in wer. alcohols. react with alcohols and a trace of acid to yield hemiacetals 10) Carboxylic acids contain the carbonyl functional group 11) Carboxylic acids are more acidic than phenols. dimers 12) Carboxylie acids have higher boiling points partially becase they fom 13) Carboxylie acids can nestralize strong acids. 14) Esters are formed from the reaction of an ether with a carbosylic acid.Explanation / Answer
3-Pentanone + Methanol ---> 3-methoxypentan-3-ol (hemiketal) ---> 3,3-dimethoxypentane (ketal) (in presence of little acid)
Pentanoic acid + Methanol ---> methyl pentanoate (ester)
Why:
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