a) Interpretation: The name of the ketone shown is to be given. Concept introduction: Ketones are named by replacing the terminal –e of the parent alkane with –one. The parent chain is the longest one that includes the ketone group and the numbering begins at the end nearer to the carbonyl carbon. If other functional groups are present the double bonded oxygen is considered as a substituent on the parent chain with the prefix –oxo. To give: The name of the ketone shown.

Question

Place the following characteristics into the box for the correct ion. Note that some of the characteristics will not be placed in either bin. Use your periodic table for assistance. Link to Periodic Table Drag the characteristics to their respective bins. ▸ View Available Hint(s) This anion could form a neutral compound by forming an ionic bond with one Ca²+. Reset Help This ion forms ionic bonds with nonmetals. This ion has a 1- charge. This is a polyatomic ion. The neutral atom from which this ion is formed is a metal. The atom from which this ion is formed gains an electron to become an ion. The atom from which this ion is formed loses an electron to become an ion. This ion has a total of 18 electrons. This ion has a total of 36 electrons. This ion has covalent bonds and a net 2- charge. This ion has a 1+ charge. Potassium ion Bromide ion Sulfate ion

Answer 1

Question

Chapter 19.1, Problem 1P

Interpretation Introduction

a)

Interpretation:

The name of the ketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. The parent chain is the longest one that includes the ketone group and the numbering begins at the end nearer to the carbonyl carbon. If other functional groups are present the double bonded oxygen is considered as a substituent on the parent chain with the prefix –oxo.

To give:

The name of the ketone shown.

Interpretation Introduction

b)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the –CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Interpretation Introduction

c)

Interpretation:

The name of the diketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. The parent chain is the longest one that includes the ketone group and the numbering begins at the end nearer to the carbonyl carbon. If other functional groups are present the double bonded oxygen is considered as a substituent on the parent chain with the prefix –oxo.

To give:

The name of the diketone shown.

Interpretation Introduction

d)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the -CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Interpretation Introduction

e)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the –CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Interpretation Introduction

f)

Interpretation:

The name of the ketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. For alicyclic ketones the number of carbons in the ring determines the parent name. The numbering starts from the carbonyl carbon and the numbering is done such a way that other functional groups and/or substituents get the lowest possible number.

To give:

The name of the ketone shown.

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Place the following characteristics into the box for the correct ion. Note that some of the characteristics will not be placed in either bin. Use your periodic table for assistance. Link to Periodic Table Drag the characteristics to their respective bins. ▸ View Available Hint(s) This anion could form a neutral compound by forming an ionic bond with one Ca²+. Reset Help This ion forms ionic bonds with nonmetals. This ion has a 1- charge. This is a polyatomic ion. The neutral atom from which this ion is formed is a metal. The atom from which this ion is formed gains an electron to become an ion. The atom from which this ion is formed loses an electron to become an ion. This ion has a total of 18 electrons. This ion has a total of 36 electrons. This ion has covalent bonds and a net 2- charge. This ion has a 1+ charge. Potassium ion Bromide ion Sulfate ion

U Consider the following graph containing line plots for the moles of Product 1 versus time (minutes) and the moles of Product 2 versus time in minutes. Choose all of the key terms/phrases that describe the plots on this graph. Check all that apply. ▸ View Available Hint(s) Slope is zero. More of Product 1 is obtained in 12 minutes. Slope has units of moles per minute. plot of minutes versus moles positive relationship between moles and minutes negative relationship between moles and minutes Slope has units of minutes per moles. More of Product 2 is obtained in 12 minutes. can be described using equation y = mx + b plot of moles versus minutes y-intercept is at (12,10). y-intercept is at the origin. Product Amount (moles) Product 1 B (12,10) Product 2 E 1 Time (minutes) A (12,5)

Solve for x, where M is molar and s is seconds. x = (9.0 × 10³ M−². s¯¹) (0.26 M)³ Enter the answer. Include units. Use the exponent key above the answer box to indicate any exponent on your units. ▸ View Available Hint(s) ΜΑ 0 ? Units Value

Answer 2

Question

Chapter 19.1, Problem 1P

Interpretation Introduction

a)

Interpretation:

The name of the ketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. The parent chain is the longest one that includes the ketone group and the numbering begins at the end nearer to the carbonyl carbon. If other functional groups are present the double bonded oxygen is considered as a substituent on the parent chain with the prefix –oxo.

To give:

The name of the ketone shown.

Interpretation Introduction

b)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the –CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Interpretation Introduction

c)

Interpretation:

The name of the diketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. The parent chain is the longest one that includes the ketone group and the numbering begins at the end nearer to the carbonyl carbon. If other functional groups are present the double bonded oxygen is considered as a substituent on the parent chain with the prefix –oxo.

To give:

The name of the diketone shown.

Interpretation Introduction

d)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the -CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Interpretation Introduction

e)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the –CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Interpretation Introduction

f)

Interpretation:

The name of the ketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. For alicyclic ketones the number of carbons in the ring determines the parent name. The numbering starts from the carbonyl carbon and the numbering is done such a way that other functional groups and/or substituents get the lowest possible number.

To give:

The name of the ketone shown.

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Answer 3

Question

Chapter 19.1, Problem 1P

Interpretation Introduction

a)

Interpretation:

The name of the ketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. The parent chain is the longest one that includes the ketone group and the numbering begins at the end nearer to the carbonyl carbon. If other functional groups are present the double bonded oxygen is considered as a substituent on the parent chain with the prefix –oxo.

To give:

The name of the ketone shown.

Interpretation Introduction

b)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the –CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Interpretation Introduction

c)

Interpretation:

The name of the diketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. The parent chain is the longest one that includes the ketone group and the numbering begins at the end nearer to the carbonyl carbon. If other functional groups are present the double bonded oxygen is considered as a substituent on the parent chain with the prefix –oxo.

To give:

The name of the diketone shown.

Interpretation Introduction

d)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the -CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Interpretation Introduction

e)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the –CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Interpretation Introduction

f)

Interpretation:

The name of the ketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. For alicyclic ketones the number of carbons in the ring determines the parent name. The numbering starts from the carbonyl carbon and the numbering is done such a way that other functional groups and/or substituents get the lowest possible number.

To give:

The name of the ketone shown.

Expert Solution & Answer

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Answer 4

Question

Chapter 19.1, Problem 1P

Interpretation Introduction

a)

Interpretation:

The name of the ketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. The parent chain is the longest one that includes the ketone group and the numbering begins at the end nearer to the carbonyl carbon. If other functional groups are present the double bonded oxygen is considered as a substituent on the parent chain with the prefix –oxo.

To give:

The name of the ketone shown.

Interpretation Introduction

b)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the –CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Interpretation Introduction

c)

Interpretation:

The name of the diketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. The parent chain is the longest one that includes the ketone group and the numbering begins at the end nearer to the carbonyl carbon. If other functional groups are present the double bonded oxygen is considered as a substituent on the parent chain with the prefix –oxo.

To give:

The name of the diketone shown.

Interpretation Introduction

d)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the -CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Interpretation Introduction

e)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the –CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Interpretation Introduction

f)

Interpretation:

The name of the ketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. For alicyclic ketones the number of carbons in the ring determines the parent name. The numbering starts from the carbonyl carbon and the numbering is done such a way that other functional groups and/or substituents get the lowest possible number.

To give:

The name of the ketone shown.

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Answer 5

Chapter 19.1, Problem 1P

Interpretation Introduction

a)

Interpretation:

The name of the ketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. The parent chain is the longest one that includes the ketone group and the numbering begins at the end nearer to the carbonyl carbon. If other functional groups are present the double bonded oxygen is considered as a substituent on the parent chain with the prefix –oxo.

To give:

The name of the ketone shown.

Interpretation Introduction

b)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the –CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Interpretation Introduction

c)

Interpretation:

The name of the diketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. The parent chain is the longest one that includes the ketone group and the numbering begins at the end nearer to the carbonyl carbon. If other functional groups are present the double bonded oxygen is considered as a substituent on the parent chain with the prefix –oxo.

To give:

The name of the diketone shown.

Interpretation Introduction

d)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the -CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Interpretation Introduction

e)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the –CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Interpretation Introduction

f)

Interpretation:

The name of the ketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. For alicyclic ketones the number of carbons in the ring determines the parent name. The numbering starts from the carbonyl carbon and the numbering is done such a way that other functional groups and/or substituents get the lowest possible number.

To give:

The name of the ketone shown.

Answer 6

Chapter 19.1, Problem 1P

Interpretation Introduction

a)

Interpretation:

The name of the ketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. The parent chain is the longest one that includes the ketone group and the numbering begins at the end nearer to the carbonyl carbon. If other functional groups are present the double bonded oxygen is considered as a substituent on the parent chain with the prefix –oxo.

To give:

The name of the ketone shown.

Answer 7

Chapter 19.1, Problem 1P

Interpretation Introduction

a)

Interpretation:

The name of the ketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. The parent chain is the longest one that includes the ketone group and the numbering begins at the end nearer to the carbonyl carbon. If other functional groups are present the double bonded oxygen is considered as a substituent on the parent chain with the prefix –oxo.

To give:

The name of the ketone shown.

Answer 8

Interpretation Introduction

b)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the –CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Answer 9

Interpretation Introduction

b)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the –CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Answer 10

Interpretation Introduction

c)

Interpretation:

The name of the diketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. The parent chain is the longest one that includes the ketone group and the numbering begins at the end nearer to the carbonyl carbon. If other functional groups are present the double bonded oxygen is considered as a substituent on the parent chain with the prefix –oxo.

To give:

The name of the diketone shown.

Answer 11

Interpretation Introduction

c)

Interpretation:

The name of the diketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. The parent chain is the longest one that includes the ketone group and the numbering begins at the end nearer to the carbonyl carbon. If other functional groups are present the double bonded oxygen is considered as a substituent on the parent chain with the prefix –oxo.

To give:

The name of the diketone shown.

Answer 12

Interpretation Introduction

d)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the -CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Answer 13

Interpretation Introduction

d)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the -CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Answer 14

Interpretation Introduction

e)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the –CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Answer 15

Interpretation Introduction

e)

Interpretation:

The name of the aldehyde shown is to be given.

Concept introduction:

Aldehydes are named by replacing the terminal –e of the parent alkane with –al. The parent chain is the longest one that includes the –CHO group and the –CHO group is numbered as carbon 1. For cyclic aldehydes in which the –CHO group is directly attached to the ring, the suffix –carbaldehyde is used.

To give:

The name of the aldehyde shown.

Answer 16

Interpretation Introduction

f)

Interpretation:

The name of the ketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. For alicyclic ketones the number of carbons in the ring determines the parent name. The numbering starts from the carbonyl carbon and the numbering is done such a way that other functional groups and/or substituents get the lowest possible number.

To give:

The name of the ketone shown.

Answer 17

Interpretation Introduction

f)

Interpretation:

The name of the ketone shown is to be given.

Concept introduction:

Ketones are named by replacing the terminal –e of the parent alkane with –one. For alicyclic ketones the number of carbons in the ring determines the parent name. The numbering starts from the carbonyl carbon and the numbering is done such a way that other functional groups and/or substituents get the lowest possible number.

To give:

The name of the ketone shown.

Answer 18

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Answer 19

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Answer 23

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Answer 29

Ch. 19.1 - Prob. 1P Ch. 19.1 - Draw structures corresponding to the following...Ch. 19.2 - Prob. 3P Ch. 19.2 - How would you carry out the following reactions?...Ch. 19.4 - Treatment of an aldehyde or ketone with cyanide...Ch. 19.4 - p-Nitrobenzaldehyde is more reactive toward...Ch. 19.5 - Prob. 7P Ch. 19.5 - The oxygen in water is primarily (99.8) 16O, but...Ch. 19.6 - Prob. 9P Ch. 19.8 - Show the products you would obtain by...

Solution Summary: The author explains that the name of the ketone shown is 2-methylpentan-3-one.

Chapter 19 Solutions