Organic Chemistry Study Guide and Solutions Manual, Books a la Carte Edition (8th Edition)
Organic Chemistry Study Guide and Solutions Manual, Books a la Carte Edition (8th Edition)
8th Edition
ISBN: 9780134649771
Author: Paula Yurkanis Bruice
Publisher: PEARSON
Question
Book Icon
Chapter 16, Problem 59P

a.

Interpretation Introduction

Interpretation:

Name the given compound.

Concept introduction:

The nomenclature of aldehydes and ketones. The functional group in the aldehydes and Ketones are carbonyl group.

Naming Aldehydes:

Aldehydes have at least one hydrogen attached to the carbonyl carbon atom.

The IUPAC naming of an aldehydes is obtained by replacing the final "e" on the name of the parent hydrocarbon with "al".

The common name of the aldehyde is substituted for "oic acid" at the end of parent hydrocarbon chain.

For example:

Organic Chemistry Study Guide and Solutions Manual, Books a la Carte Edition (8th Edition), Chapter 16, Problem 59P , additional homework tip  1

Naming Ketones:

Carbonyl carbon atom attached to the two oxygen atoms.

The IUPAC name of a ketones are obtained by replacing the "e" on the end of the parent hydrocarbon with "one".

Only few ketones have common name.

For example:

Organic Chemistry Study Guide and Solutions Manual, Books a la Carte Edition (8th Edition), Chapter 16, Problem 59P , additional homework tip  2

b.

Interpretation Introduction

Interpretation:

Name the given compound.

Concept introduction:

Naming Aldehydes:

Aldehydes have at least one hydrogen attached to the carbonyl carbon atom.

The IUPAC naming of an aldehydes is obtained by replacing the final "e" on the name of the parent hydrocarbon with "al".

The common name of the aldehyde is substituted for "oic acid" at the end of parent hydrocarbon chain.

For example:

Organic Chemistry Study Guide and Solutions Manual, Books a la Carte Edition (8th Edition), Chapter 16, Problem 59P , additional homework tip  3

Naming Ketones:

Carbonyl carbon atom attached to the two oxygen atoms.

The IUPAC name of a ketones are obtained by replacing the "e" on the end of the parent hydrocarbon with "one".

Only few ketones have common name.

For example:

Organic Chemistry Study Guide and Solutions Manual, Books a la Carte Edition (8th Edition), Chapter 16, Problem 59P , additional homework tip  4

c.

Interpretation Introduction

Interpretation:

Name the given compound.

Concept introduction:

Naming Aldehydes:

Aldehydes have at least one hydrogen attached to the carbonyl carbon atom.

The IUPAC naming of an aldehydes is obtained by replacing the final "e" on the name of the parent hydrocarbon with "al".

The common name of the aldehyde is substituted for "oic acid" at the end of parent hydrocarbon chain.

For example:

Organic Chemistry Study Guide and Solutions Manual, Books a la Carte Edition (8th Edition), Chapter 16, Problem 59P , additional homework tip  5

Naming Ketones:

Carbonyl carbon atom attached to the two oxygen atoms.

The IUPAC name of a ketones are obtained by replacing the "e" on the end of the parent hydrocarbon with "one".

Only few ketones have common name.

For example:

Organic Chemistry Study Guide and Solutions Manual, Books a la Carte Edition (8th Edition), Chapter 16, Problem 59P , additional homework tip  6

d.

Interpretation Introduction

Interpretation:

Name the given compound.

Concept introduction:

Naming Aldehydes:

Aldehydes have at least one hydrogen attached to the carbonyl carbon atom.

The IUPAC naming of an aldehydes is obtained by replacing the final "e" on the name of the parent hydrocarbon with "al".

The common name of the aldehyde is substituted for "oic acid" at the end of parent hydrocarbon chain.

For example:

Organic Chemistry Study Guide and Solutions Manual, Books a la Carte Edition (8th Edition), Chapter 16, Problem 59P , additional homework tip  7

Naming Ketones:

Carbonyl carbon atom attached to the two oxygen atoms.

The IUPAC name of a ketones are obtained by replacing the "e" on the end of the parent hydrocarbon with "one".

Only few ketones have common name.

For example:

Organic Chemistry Study Guide and Solutions Manual, Books a la Carte Edition (8th Edition), Chapter 16, Problem 59P , additional homework tip  8

Blurred answer
Students have asked these similar questions
When 15.00 mL of 3.00 M NaOH was mixed in a calorimeter with 12.80 mL of 3.00 M HCl, both initially at room temperature (22.00 C), the temperature increased to 29.30 C. The resultant salt solution had a mass of 27.80 g and a specific heat capacity of 3.74 J/Kg. What is heat capacity of the calorimeter (in J/C)? Note: The molar enthalpy of neutralization per mole of HCl is -55.84 kJ/mol.
When 15.00 mL of 3.00 M NaOH was mixed in a calorimeter with 12.80 mL of 3.00 M HCl, both initially at room temperature (22.00 C), the temperature increased to 29.30 C. The resultant salt solution had a mass of 27.80 g and a specific heat capacity of 3.74 J/Kg. What is heat capacity of the calorimeter (in J/C)? Note: The molar enthalpy of neutralization per mole of HCl is -55.84 kJ/mol.   Which experimental number must be initialled by the Lab TA for the first run of Part 1 of the experiment? a) the heat capacity of the calorimeter b) Mass of sample c) Ti d) The molarity of the HCl e) Tf
Predict products for the Following organic rxn/s by writing the structurels of the correct products. Write above the line provided" your answer D2 ①CH3(CH2) 5 CH3 + D₂ (adequate)" + 2 mited) 19 Spark Spark por every item. 4 CH 3 11 3 CH 3 (CH2) 4 C-H + CH3OH CH2 CH3 + CH3 CH2OH 0 CH3 fou + KMnDy→ C43 + 2 KMn Dy→→ C-OH ") 0 C-OH 1110 (4.) 9+3 =C CH3 + HNO 3 0 + Heat> + CH3 C-OH + Heat CH2CH3 - 3 2 + D Heat H 3 CH 3 CH₂ CH₂ C = CH + 2 H₂ → 2 2

Chapter 16 Solutions

Organic Chemistry Study Guide and Solutions Manual, Books a la Carte Edition (8th Edition)

Ch. 16.4 - Show how the following compounds can be...Ch. 16.4 - Prob. 13PCh. 16.4 - Prob. 14PCh. 16.4 - In the mechanism for cyanohydrin formation, why is...Ch. 16.4 - Prob. 16PCh. 16.4 - Prob. 17PCh. 16.4 - Show two ways to convert an alkyl halide into a...Ch. 16.5 - Prob. 20PCh. 16.5 - Prob. 21PCh. 16.5 - Prob. 22PCh. 16.5 - Prob. 23PCh. 16.6 - Prob. 24PCh. 16.7 - What reducing agents should be used to obtain the...Ch. 16.7 - Prob. 26PCh. 16.8 - Prob. 27PCh. 16.8 - Prob. 28PCh. 16.8 - Prob. 29PCh. 16.8 - The pKa of protonated acetone is about 7.5. and...Ch. 16.8 - Prob. 31PCh. 16.8 - Prob. 32PCh. 16.8 - Prob. 33PCh. 16.8 - Excess ammonia must be used when a primary amine...Ch. 16.8 - The compounds commonly known as amino acids are...Ch. 16.9 - Hydration of an aldehyde is also catalyzed by...Ch. 16.9 - Which ketone forms the most hydrate in an aqueous...Ch. 16.9 - When trichloroacetaldehyde is dissolved in water,...Ch. 16.9 - Which of the following are a. hermiacetals? b....Ch. 16.9 - Prob. 40PCh. 16.9 - Explain why an acetal can be isolated but most...Ch. 16.10 - Prob. 42PCh. 16.10 - Prob. 43PCh. 16.10 - What products would be formed from the proceedings...Ch. 16.10 - a. In a six-step synthesis, what is the yield of...Ch. 16.10 - Show how each of the following compounds could be...Ch. 16.12 - Prob. 47PCh. 16.13 - Prob. 49PCh. 16.14 - Prob. 50PCh. 16.15 - Prob. 51PCh. 16.16 - Prob. 52PCh. 16 - Draw the structure for each of the following: a....Ch. 16 - Prob. 54PCh. 16 - Prob. 55PCh. 16 - Prob. 56PCh. 16 - a. Show the reagents required to form the primary...Ch. 16 - Prob. 58PCh. 16 - Prob. 59PCh. 16 - Using cyclohexanone as the starting material,...Ch. 16 - Propose a mechanism for each of the following...Ch. 16 - Show how each of the following compounds can be...Ch. 16 - Fill in the boxes:Ch. 16 - Prob. 64PCh. 16 - Identify A through O:Ch. 16 - Prob. 66PCh. 16 - Prob. 67PCh. 16 - Prob. 68PCh. 16 - How many signals would the product of the...Ch. 16 - Prob. 70PCh. 16 - Prob. 71PCh. 16 - Prob. 72PCh. 16 - Prob. 73PCh. 16 - Prob. 74PCh. 16 - Prob. 75PCh. 16 - Prob. 76PCh. 16 - Prob. 77PCh. 16 - Prob. 78PCh. 16 - Draw structure for A-D for each of the following:Ch. 16 - Prob. 80PCh. 16 - a. Propose a mechanism for the following reaction:...Ch. 16 - Prob. 82PCh. 16 - A compound gives the following IR spectrum. Upon...Ch. 16 - How can be following compounds be prepared from...Ch. 16 - Prob. 85PCh. 16 - Prob. 86PCh. 16 - Prob. 87PCh. 16 - In the presence of an acid catalyst, acetaldehyde...Ch. 16 - Prob. 89PCh. 16 - Prob. 90PCh. 16 - Prob. 91PCh. 16 - A compound reacts with methylmagnesium bromide...Ch. 16 - Show how each of the following compounds can be...Ch. 16 - Prob. 94PCh. 16 - The pKa values of the carboxylic acid groups of...Ch. 16 - The Baylis-Hillman reaction is a DABCO...Ch. 16 - Prob. 97PCh. 16 - Prob. 98P
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning
Text book image
EBK A SMALL SCALE APPROACH TO ORGANIC L
Chemistry
ISBN:9781305446021
Author:Lampman
Publisher:CENGAGE LEARNING - CONSIGNMENT
Text book image
Fundamentals Of Analytical Chemistry
Chemistry
ISBN:9781285640686
Author:Skoog
Publisher:Cengage
Text book image
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning
Text book image
Introduction to General, Organic and Biochemistry
Chemistry
ISBN:9781285869759
Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher:Cengage Learning