IUPAC name for the given propanoic acid salt has to be chosen from the given options. Concept Introduction: Carboxylic acid salts when treated with a strong acid produces carboxylic acid as the product. Carboxylic acid salts contain two ions. They are a negative carboxylate ion and a positive ion. When naming the carboxylic acid salt, the positive ion is named first that is followed by the carboxylate name. The carboxylate is named from the parent carboxylic acid by replacing the suffix “-ic acid” with “-ate”.

Question

Consider the following SN 2 reaction: مار + Br H₂O acetone + Br OH What effect would each of the following changes have on the rate of this reaction. Select the single best answer for each part. Part 1 of 3 If the substrate was changed to: The rate would Br O increase O decrease O remain unchanged Part 2 of 3 × S If the nucleophile was changed to OH, the rate would: O increase O decrease O remain unchanged Part 3 of 3 If the solvent was changed to ethanol, the rate would: Increase O decrease O remain unchanged 2 ol Ar

Answer 1

Question

Chapter 16.8, Problem 4QQ

Interpretation Introduction

Interpretation:

IUPAC name for the given propanoic acid salt has to be chosen from the given options.

Concept Introduction:

Carboxylic acid salts when treated with a strong acid produces carboxylic acid as the product. Carboxylic acid salts contain two ions. They are a negative carboxylate ion and a positive ion. When naming the carboxylic acid salt, the positive ion is named first that is followed by the carboxylate name. The carboxylate is named from the parent carboxylic acid by replacing the suffix “-ic acid” with “-ate”.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Students have asked these similar questions

Consider the following SN 2 reaction: مار + Br H₂O acetone + Br OH What effect would each of the following changes have on the rate of this reaction. Select the single best answer for each part. Part 1 of 3 If the substrate was changed to: The rate would Br O increase O decrease O remain unchanged Part 2 of 3 × S If the nucleophile was changed to OH, the rate would: O increase O decrease O remain unchanged Part 3 of 3 If the solvent was changed to ethanol, the rate would: Increase O decrease O remain unchanged 2 ol Ar

Consider the following nucleophilic substitution reaction. The compound listed above the arrow is the solvent for the reaction. If nothing is listed over the arrow, then the nucleophile is also the solvent for the reaction. Part: 0/2 Part 1 of 2 Br acetone + I What is the correct mechanism for the reaction? Select the single best answer. OSN 1 OSN 2 X Part: 1/2 Part 2 of 2 Draw the products for the reaction. Include both the major organic product and the inorganic product. If more than one stereoisomer is possible, draw only one stereoisomer. Include stereochemistry where relevant. Click and drag to start drawing a structure. Х 5 ☐

Triethyloxonium tetrafluoroborate reacts with ethanol (CH3CH2OH) to give diethyl ether (CH3CH2OCH2CH3). BF triethyloxonium tetrafluoroborate Which equation, including the curved arrows, best represents the rate-determining step in the mechanism? Select the single best answer. O OH CH3CH2 OH + H. 0+ CH₂H₂ :0 + 0+ ж + H + :0: 0 C