7th Edition

ISBN: 9780321939036

Author: Bruice

Publisher: PEARSON

Concept explainers

The electromagnetic radiation or frequency is classified into radio-waves, micro-waves, infrared, visible, ultraviolet, X-rays and gamma rays. The infrared spectra emission refers to the portion between the visible and the microwave areas of electromagne…

IR Spectrum Of Cyclohexanone

It is the analysis of the structure of cyclohexaone using IR data interpretation.

IR Spectrum Of Anisole

Interpretation of anisole using IR spectrum obtained from IR analysis.

IR Spectroscopy

Infrared (IR) or vibrational spectroscopy is a method used for analyzing the particle's vibratory transformations. This is one of the very popular spectroscopic approaches employed by inorganic as well as organic laboratories because it is helpful in eva…

Videos

Textbook Question

Chapter 16.2, Problem 7P

There are three carbon-oxygen bonds in methyl acetate.

a. What are their relative bond lengths?
b. What are the relative infrared (IR) stretching frequencies of these bonds?

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Chapter 16.2, Problem 6P

Chapter 16.2, Problem 8P

Students have asked these similar questions

There are three carbon–oxygen bonds in methyl acetate. a. What are their relative bond lengths? b. What are the relative infrared (IR) stretching frequencies of these bonds?

a) which bond is present in alcohols but not alkanes? b) is this band strong or weak (in terms of spectra)? c) what is different about C=O and O-H bonds compared with C=C or C≡C bonds that show weaker signals?

5- In each part, choose the structure that best adapts to the infrared spectrum

Chapter 16 Solutions

Organic Chemistry (Package) (Looseleaf)

Ch. 16.1 - The aromas of many flowers and fruits are due to...Ch. 16.1 - Prob. 2P Ch. 16.1 - Name the following:Ch. 16.1 - Prob. 4P Ch. 16.2 - Prob. 5P Ch. 16.2 - Which is longer, the carbon-oxygen single bond in...Ch. 16.2 - There are three carbon-oxygen bonds in methyl...Ch. 16.2 - Prob. 8P Ch. 16.4 - Prob. 9P Ch. 16.4 - Prob. 10P

Ch. 16.5 - a. What is the product of the reaction of acetyl...Ch. 16.6 - a. Which compound has the stretching vibration for...Ch. 16.6 - Using the pKa values listed in Table 15.1, predict...Ch. 16.6 - Is the following statement true or false? If the...Ch. 16.7 - What is the product of an acyl substitution...Ch. 16.8 - PROBLEM 16 Starting with acetyl chloride, what...Ch. 16.8 - Prob. 18P Ch. 16.9 - We saw that it is necessary to use excess amine in...Ch. 16.9 - Prob. 20P Ch. 16.9 - a. state three factors that cause the uncatalyzed...Ch. 16.10 - Prob. 23P Ch. 16.10 - Using the mechanism for the acid-catalyzed...Ch. 16.10 - Prob. 25P Ch. 16.10 - Prob. 27P Ch. 16.10 - Write the mechanism for the acid-catalyzed...Ch. 16.10 - Write the mechanism for the acid-catalyzed...Ch. 16.11 - Prob. 30P Ch. 16.12 - Prob. 31P Ch. 16.12 - Prob. 32P Ch. 16.13 - Prob. 34P Ch. 16.13 - Which has a higher melting point, glyceryl...Ch. 16.13 - Draw the structure of an optically inactive fat...Ch. 16.13 - Draw the structure of an optically active fat...Ch. 16.14 - Show how each of the following esters could he...Ch. 16.14 - Prob. 39P Ch. 16.15 - Prob. 40P Ch. 16.15 - Which of the following reactions leads to the...Ch. 16.16 - Prob. 42P Ch. 16.16 - Prob. 43P Ch. 16.18 - Prob. 44P Ch. 16.18 - Prob. 45P Ch. 16.19 - Prob. 46P Ch. 16.19 - Which alkyl halides from the carboxylic acids...Ch. 16.20 - Prob. 49P Ch. 16.20 - Prob. 50P Ch. 16.20 - Prob. 51P Ch. 16.21 - Prob. 52P Ch. 16.21 - Prob. 53P Ch. 16.22 - How could you synthesize the following compounds...Ch. 16 - Prob. 55P Ch. 16 - Name the following:Ch. 16 - Prob. 57P Ch. 16 - What compound are obtained from the fallowing...Ch. 16 - a. Rank the following esters in order of...Ch. 16 - Because bromocyclohexane is a secondary alkyl...Ch. 16 - a. Which compound would you expect to have a...Ch. 16 - How could you use 1H NMR spectroscopy to...Ch. 16 - Prob. 63P Ch. 16 - a. When a carboxylic acid is dissolved in...Ch. 16 - Rank the following compounds in order of...Ch. 16 - Prob. 66P Ch. 16 - Prob. 67P Ch. 16 - Prob. 68P Ch. 16 - A compound with molecular formula C5H10O2 gives...Ch. 16 - Prob. 70P Ch. 16 - Prob. 71P Ch. 16 - Prob. 72P Ch. 16 - Two products, A and B, are obtained from the...Ch. 16 - Prob. 74P Ch. 16 - Prob. 75P Ch. 16 - Prob. 76P Ch. 16 - Prob. 77P Ch. 16 - When treated with an equivalent of methanol,...Ch. 16 - a. Identify the two products obtained from the...Ch. 16 - Prob. 80P Ch. 16 - Identity the major and minor products of the...Ch. 16 - Prob. 82P Ch. 16 - When a compound with molecular formula C11H14O2...Ch. 16 - Prob. 84P Ch. 16 - Prob. 85P Ch. 16 - The 1H NMR spectra for two esters with molecular...Ch. 16 - Show how the following compounds could be prepared...Ch. 16 - Prob. 88P Ch. 16 - Prob. 89P Ch. 16 - Prob. 90P Ch. 16 - The intermediate shown here is formed during the...Ch. 16 - Prob. 92P Ch. 16 - Propose a mechanism that accounts for the...Ch. 16 - Catalytic antibodies catalyze a reaction by...Ch. 16 - Prob. 95P

Knowledge Booster

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.

There are three carbon-oxygen bonds in methyl acetate. a. What are their relative bond lengths? b. What are the relative infrared (IR) stretching frequencies of these bonds?

Concept explainers

Videos

Want to see the full answer?

Chapter 16 Solutions