why do tertiary alcohols ionize readily in acidic media

Which of the following would be most miscible in n-nonane, CH3CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH3? formic acid, COOH ammonia, NH3 n-butane, CH3CH₂CH₂CH3 n-butanol, CH3CH₂CH₂CH₂OH

Give detailed Solution with explanation needed..don't give Handwritten answer

Consider propanoic (CH3CH2CH2CO2H) acid and pentanoic (CH3CH2CH2CH2CO2H) acid and the corresponding alcohols with the same number of carbons, propanol (CH3CH2CH2COH) and pentanol (CH3CH2CH2CH2COH). Select the class of compound that is more soluble. {one answer] Select the best explanation for your answer to the previous question. [a second answer] Group of answer choices a. The solubility of alcohols in water decreases with increasing chain length. b. Propanoic acid and pentanoic acid are more soluble in water than the corresponding alcohol. c. Carboxylic acids are generally more soluble in water than alcohols of the same chain length because of increased hydrogen bonding with the -COOH functional group.  d. Propanol and pentanol are more soluble in water than the corresponding carboxylic acid e. The solubility of carboxylic acids in water decreases with increasing chain length. f. Alcohols are generally more soluble in water than carboxylic acids of the same…