The structure, name and the class belongs for the product fromed from the reaction between butanoic acid and methylamine should be given. The balanced chemical equation for the reaction of butanoic acid andmethylamine should be written. Concept introduction: Amide Formation: Amide is formed when a carboxylic acid reacts with an amine or ammonia. Here, the − O H group is attached to the carbonyl carbon atom of the carboxylic acid is being replaced by − N H 2 , − N H R ' or − N R ' 2 group in the an amine or ammonia forming amide and water. Chemical equation is the representation of a chemical reaction , in which the reactants and products of the reactions are represented left and right side of an arrow respectively by using their respective chemical formulas. Balanced chemical equation of a reaction is written according to law of conservation of mass.

Question

13. (11pts total) Consider the arrows pointing at three different carbon-carbon bonds in the molecule depicted below. Bond B Bond A Bond C a. (2pts) Which bond between A-C is weakest? Which is strongest? Place answers in appropriate boxes. Weakest Bond Strongest Bond b. (4pts) Consider the relative stability of all cleavage products that form when bonds A, B, AND C are homolytically cleaved/broken. Hint: cleavage products of bonds A, B, and C are all carbon radicals. i. Which ONE cleavage product is the most stable? A condensed or bond line representation is fine. ii. Which ONE cleavage product is the least stable? A condensed or bond line representation is fine. c. (5pts) Use principles discussed in lecture, supported by relevant structures, to succinctly explain the why your part b (i) radical is more stable than your part b(ii) radical. Written explanation can be no more than one-two succinct sentence(s)! Google

Answer 1

Question

Chapter 23, Problem 59PS

Interpretation Introduction

Interpretation: The structure, name and the class belongs for the product fromed from the reaction between butanoic acid and methylamine should be given. The balanced chemical equation for the reaction of butanoic acid andmethylamine should be written.

Concept introduction:

Amide Formation: Amide is formed when a carboxylic acid reacts with an amine or ammonia.

Here, the −OH group is attached to the carbonyl carbon atom of the carboxylic acid is being replaced by −NH2, −NHR' or −NR'2 group in the an amine or ammonia forming amide and water.

Chemical equation is the representation of a chemical reaction, in which the reactants and products of the reactions are represented left and right side of an arrow respectively by using their respective chemical formulas.

Balanced chemical equation of a reaction is written according to law of conservation of mass.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Students have asked these similar questions

13. (11pts total) Consider the arrows pointing at three different carbon-carbon bonds in the molecule depicted below. Bond B Bond A Bond C a. (2pts) Which bond between A-C is weakest? Which is strongest? Place answers in appropriate boxes. Weakest Bond Strongest Bond b. (4pts) Consider the relative stability of all cleavage products that form when bonds A, B, AND C are homolytically cleaved/broken. Hint: cleavage products of bonds A, B, and C are all carbon radicals. i. Which ONE cleavage product is the most stable? A condensed or bond line representation is fine. ii. Which ONE cleavage product is the least stable? A condensed or bond line representation is fine. c. (5pts) Use principles discussed in lecture, supported by relevant structures, to succinctly explain the why your part b (i) radical is more stable than your part b(ii) radical. Written explanation can be no more than one-two succinct sentence(s)! Google

Print Last Name, First Name Initial Statifically more chances to abstract one of these 6H 11. (10pts total) Consider the radical chlorination of 1,3-diethylcyclohexane depicted below. 4 4th total • 6H total 래 • 4H total 21 total ZH 2H Statistical H < 3° C-H weakest - product abstraction here bund leads to thermo favored a) (6pts) How many unique mono-chlorinated products can be formed and what are the structures for the thermodynamically and statistically favored products? Product 6 Number of Unique Mono-Chlorinated Products Thermodynamically Favored Product Statistically Favored Product b) (4pts) Draw the arrow pushing mechanism for the FIRST propagation step (p-1) for the formation of the thermodynamically favored product. Only draw the p-1 step. You do not need to include lone pairs of electrons. No enthalpy calculation necessary H H-Cl Waterfox

10. (5pts) Provide the complete arrow pushing mechanism for the chemical transformation → depicted below Use proper curved arrow notation that explicitly illustrates all bonds being broken, and all bonds formed in the transformation. Also, be sure to include all lone pairs and formal charges on all atoms involved in the flow of electrons. CH3O II HA H CH3O-H H ①