ORGANIC CHEMISTRY SAPLING ACCESS + ETEX
ORGANIC CHEMISTRY SAPLING ACCESS + ETEX
6th Edition
ISBN: 9781319306977
Author: LOUDON
Publisher: INTER MAC
bartleby

Concept explainers

Question
Book Icon
Chapter 17, Problem 17.47AP
Interpretation Introduction

(a)

Interpretation:

The curved-arrow mechanism for the reaction of 2-hexyne with strong base (NHCH2CH2CH2NH2) is to be predicted. The explanation for the fact that the corresponding reaction is irreversible reaction is to be stated.

Concept introduction:

The isomerization process of converting internal alkynes into terminal alkynes is known as acetylene zipper reaction. The acetylene zipper reaction required a strong base. A diamine ion is used in the reaction to transfer proton from one carbon atom to another carbon atom.

Interpretation Introduction

(b)

Interpretation:

The product of reaction of 3-methyl-4-octyne with strong base (NHCH2CH2CH2NH2) is to be predicted.

Concept introduction:

The isomerization process of converting internal alkynes into terminal alkynes is known as acetylene zipper reaction. The acetylene zipper reaction required a strong base. A diamine ion is used in the reaction to transfer proton from one carbon atom to another carbon atom.

Blurred answer
Students have asked these similar questions
יווי 10 20 30 40 50 60 70 3.5 3 2.5 2 1.5 1 [ppm] 3.5 3 2.5 2 1.5 1 6 [ppm] 1 1.5 -2.5 3.5
2H2S(g)+3O2(g)→2SO2(g)+2H2O(g) A 1.2mol sample of H2S(g) is combined with excess O2(g), and the reaction goes to completion. Question   Which of the following predicts the theoretical yield of SO2(g) from the reaction?     Responses 1.2 g Answer A: 1.2 grams A 41 g Answer B: 41 grams B 77 g Answer C: 77 grams C 154 g Answer D: 154 grams D
Part VII. Below are the 'HNMR, 13 C-NMR, COSY 2D- NMR, and HSQC 2D-NMR (similar with HETCOR but axes are reversed) spectra of an organic compound with molecular formula C6H1003 - Assign chemical shift values to the H and c atoms of the compound. Find the structure. Show complete solutions. Predicted 1H NMR Spectrum 4.7 4.6 4.5 4.4 4.3 4.2 4.1 4.0 3.9 3.8 3.7 3.6 3.5 3.4 3.3 3.2 3.1 3.0 2.9 2.8 2.7 2.6 2.5 2.4 2.3 2.2 2.1 2.0 1.9 1.8 1.7 1.6 1.5 1.4 1.3 1.2 1.1 f1 (ppm) Predicted 13C NMR Spectrum 100 f1 (ppm) 30 220 210 200 190 180 170 160 150 140 130 120 110 90 80 70 -26 60 50 40 46 30 20 115 10 1.0 0.9 0.8 0 -10
Knowledge Booster
Background pattern image
Chemistry
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Macroscale and Microscale Organic Experiments
Chemistry
ISBN:9781305577190
Author:Kenneth L. Williamson, Katherine M. Masters
Publisher:Brooks Cole
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning