If a nonpolar carboxylic acid donates a proton to a base, which of the following results is true? The carboxylic acid becomes a negative ion. The ion is more soluble in water than the original carboxylic acid. The carboxylic acid becomes a positive ion. The ion is more soluble in water than the original carboxylic acid. The carboxylic acid becomes a negative ion. The ion is less soluble in water than the original carboxylic acid. The carboxylic acid becomes a positive ion. The ion is less soluble in water than the original carboxylic acid.

If a nonpolar carboxylic acid donates a proton to a base, which of the following results is true? The carboxylic acid becomes a negative ion. The ion is more soluble in water than the original carboxylic acid. The carboxylic acid becomes a positive ion. The ion is more soluble in water than the original carboxylic acid. The carboxylic acid becomes a negative ion. The ion is less soluble in water than the original carboxylic acid. The carboxylic acid becomes a positive ion. The ion is less soluble in water than the original carboxylic acid.

Chemistry: The Molecular Science

5th Edition

ISBN:9781285199047

Author:John W. Moore, Conrad L. Stanitski

Publisher:John W. Moore, Conrad L. Stanitski

Chapter14: Acids And Bases

Section: Chapter Questions

Problem 38QRT

See similar textbooks

Similar questions

which compound(s) would remain in an organic phase if we used aqueous NaOH? the neutral compund the basic compound the acid compound
Given 4-methylhexanoic acid1. How will the acid be deprotonated if the pH in the solution is adjusted so that the pH> pKa? 2. How will the acid be deprotonated if the pH in the solution is adjusted so that the pH = pKa? 3. How will the acid be deprotonated if the pH the solution is adjusted so that pH <pKa?
An unknown compound, X, is thought to have a carboxyl group with a p?a of 2.5 and a second ionizable group with a p?a between 5.0 and 8.0. When 50.0 mL of 0.2 M NaOH is added to 75.0 mL of a 0.2 M solution of X at pH 2.5, the pH increases to 7.13. Calculate the p?a of the second ionizable group of X.
Which of the following molecules is the most acidic? A. 3-chloroacetic acid B. 2-chloroacetic acid C. trichloroacetic acid D. trifluoroacetic acid E. triliodoacetic acid
A carboxylic acid has two oxygen atoms, each with two nonbonding pairs of electrons.(a) Draw the resonance forms of a carboxylic acid that is protonated on the hydroxyoxygen atom.(b) Compare the resonance forms with those given previously for an acid protonated on thecarbonyl oxygen atom
Select the stronger acid from pair and explain your reasoning. For stronger acid, write a structural formula for its conjugate base. Q.)CH3OH or CH3COOH
Compare the acidities of same concentrations of acetic acid, chloroacetic acid, and trichloroacetic acid. (0.1M acetic acid, 0.1M chloroacetic acid 0.1M trichloroacetic acid)
a.) For which of the following compounds is it hazardous to breathe dust/vapor /fumes: acetylsalicylic acid, salicylic acid, acetic anhydride, acetic acid, phosphoric acid? b.) Based on the boiling point or melting point of the compounds, which are you most likely to inhale accidentally? c.) Based on GHS hazard information, which would be most dangerous to inhale? d.) Of all these chemicals, which is most important to handle in a fume hood?
can someone help with this question, please draw clear. thanks
Draw the structure of the conjugate base that will be formed when 1 mole of HOCH2CO2H reacts with 1 mole of CH3CH2CH2Li.
The next set of questions are assertion type: There are two statements in a sentence. Choose from the options A-E if A. Both statements are true and related B. Both statements are true but not related C. The first statement is true and the second statement is false D. The first statement is false and the second statement is true E. Both statements are false Quartenary ammonium salts with hydrocarbon chains are used as detergent BECAUSE the presence of hydrophobic tail and ionic head facilitates its detergent action. Hofmann elimination is a reaction between an unsubstituted amide and an alkaline solution of bromine BECAUSEthe advantage of Hofmann rearrangement is that it yields pure primary amines Nitriles undergo catalytic hydrogenation or reduction with LiAlH4to yield primary amines BECAUSE this reaction is a technique for shortening carbon chain in an amine.
H2PO41- + HS1- -> HPO42- + H2S In the reaction, H2PO41- is acting as a Bronsted acid In the reaction, H2S is a Bronsted base None of the above. In the reaction, HS1- is acting as a Bronsted acid In the reaction, HPO42- is acting as a Bronsted acid