(a) Interpretation: The IUPAC name for the following alkene should be determined: Concept Introduction: Alkenes are named in the same way as alkanes , but the alkenes are identified by the suffix −ene, replaced instead of the ending of the name of the parent alkane. The longest carbon chain should be numbered in a way that gives the double bond the lower number. Then the compound should be named using the first number assigned to the double bond. The names of the substituents should be written first in the alphabetic order with their position on the chain.

Question

Want to see the full answer?

Answer 1

Question

Chapter 13.2, Problem 13.3PP

Interpretation Introduction

(a)

Interpretation:

The IUPAC name for the following alkene should be determined:

Concept Introduction:

Alkenes are named in the same way as alkanes, but the alkenes are identified by the suffix −ene, replaced instead of the ending of the name of the parent alkane. The longest carbon chain should be numbered in a way that gives the double bond the lower number. Then the compound should be named using the first number assigned to the double bond. The names of the substituents should be written first in the alphabetic order with their position on the chain.

Interpretation Introduction

(b)

Interpretation:

The IUPAC name for the following alkene should be determined:

Concept Introduction:

Alkenes are named in the same way as alkanes, but the alkenes are identified by the suffix −ene, replaced instead of the ending of the name of the parent alkane. The longest carbon chain should be numbered in a way that gives the double bond the lower number. Then the compound should be named using the first number assigned to the double bond. The names of the substituents should be written first in the alphabetic order with their position on the chain.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Please correct answer and don't use hand rating

Wavelength (nm) I'm not sure what equation I can come up with other than the one generated with my graph. Can you please show me the calculations that were used to find this equation? Give an equation that relates energy to wavelength. Explain how you arrived at your equation. Wavelength Energy (kJ/mol) (nm) 350 341.8 420 284.8 470 254.5 530 225.7 580 206.3 620 192.9 700 170.9 750 159.5 Energy vs. Wavelength (Graph 1) 400 350 y=-0.4367x+470.82 300 250 200 150 100 50 O 0 100 200 300 400 500 600 700 800 Energy (kJ/mol)

6. For the following molecules: draw Lewis dot-structures; use VSEPR method to determine geometries of the following molecules/ions. Are the central atoms in these molecules/ions considered of normal valency, or are they hypervalent? (please read paragraph 2.6) a) BrF3 (6 points) b) BrF4 c) IF₂ 4

Answer 2

Question

Chapter 13.2, Problem 13.3PP

Interpretation Introduction

(a)

Interpretation:

The IUPAC name for the following alkene should be determined:

Concept Introduction:

Alkenes are named in the same way as alkanes, but the alkenes are identified by the suffix −ene, replaced instead of the ending of the name of the parent alkane. The longest carbon chain should be numbered in a way that gives the double bond the lower number. Then the compound should be named using the first number assigned to the double bond. The names of the substituents should be written first in the alphabetic order with their position on the chain.

Interpretation Introduction

(b)

Interpretation:

The IUPAC name for the following alkene should be determined:

Concept Introduction:

Alkenes are named in the same way as alkanes, but the alkenes are identified by the suffix −ene, replaced instead of the ending of the name of the parent alkane. The longest carbon chain should be numbered in a way that gives the double bond the lower number. Then the compound should be named using the first number assigned to the double bond. The names of the substituents should be written first in the alphabetic order with their position on the chain.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 13.2, Problem 13.3PP

Interpretation Introduction

(a)

Interpretation:

The IUPAC name for the following alkene should be determined:

Concept Introduction:

Alkenes are named in the same way as alkanes, but the alkenes are identified by the suffix −ene, replaced instead of the ending of the name of the parent alkane. The longest carbon chain should be numbered in a way that gives the double bond the lower number. Then the compound should be named using the first number assigned to the double bond. The names of the substituents should be written first in the alphabetic order with their position on the chain.

Interpretation Introduction

(b)

Interpretation:

The IUPAC name for the following alkene should be determined:

Concept Introduction:

Alkenes are named in the same way as alkanes, but the alkenes are identified by the suffix −ene, replaced instead of the ending of the name of the parent alkane. The longest carbon chain should be numbered in a way that gives the double bond the lower number. Then the compound should be named using the first number assigned to the double bond. The names of the substituents should be written first in the alphabetic order with their position on the chain.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 13.2, Problem 13.3PP

Interpretation Introduction

(a)

Interpretation:

The IUPAC name for the following alkene should be determined:

Concept Introduction:

Alkenes are named in the same way as alkanes, but the alkenes are identified by the suffix −ene, replaced instead of the ending of the name of the parent alkane. The longest carbon chain should be numbered in a way that gives the double bond the lower number. Then the compound should be named using the first number assigned to the double bond. The names of the substituents should be written first in the alphabetic order with their position on the chain.

Interpretation Introduction

(b)

Interpretation:

The IUPAC name for the following alkene should be determined:

Concept Introduction:

Alkenes are named in the same way as alkanes, but the alkenes are identified by the suffix −ene, replaced instead of the ending of the name of the parent alkane. The longest carbon chain should be numbered in a way that gives the double bond the lower number. Then the compound should be named using the first number assigned to the double bond. The names of the substituents should be written first in the alphabetic order with their position on the chain.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 13.2, Problem 13.3PP

Interpretation Introduction

(a)

Interpretation:

The IUPAC name for the following alkene should be determined:

Concept Introduction:

Alkenes are named in the same way as alkanes, but the alkenes are identified by the suffix −ene, replaced instead of the ending of the name of the parent alkane. The longest carbon chain should be numbered in a way that gives the double bond the lower number. Then the compound should be named using the first number assigned to the double bond. The names of the substituents should be written first in the alphabetic order with their position on the chain.

Interpretation Introduction

(b)

Interpretation:

The IUPAC name for the following alkene should be determined:

Concept Introduction:

Alkenes are named in the same way as alkanes, but the alkenes are identified by the suffix −ene, replaced instead of the ending of the name of the parent alkane. The longest carbon chain should be numbered in a way that gives the double bond the lower number. Then the compound should be named using the first number assigned to the double bond. The names of the substituents should be written first in the alphabetic order with their position on the chain.

Answer 6

Chapter 13.2, Problem 13.3PP

Interpretation Introduction

(a)

Interpretation:

The IUPAC name for the following alkene should be determined:

Concept Introduction:

Alkenes are named in the same way as alkanes, but the alkenes are identified by the suffix −ene, replaced instead of the ending of the name of the parent alkane. The longest carbon chain should be numbered in a way that gives the double bond the lower number. Then the compound should be named using the first number assigned to the double bond. The names of the substituents should be written first in the alphabetic order with their position on the chain.

Answer 7

Chapter 13.2, Problem 13.3PP

Interpretation Introduction

(a)

Interpretation:

The IUPAC name for the following alkene should be determined:

Concept Introduction:

Alkenes are named in the same way as alkanes, but the alkenes are identified by the suffix −ene, replaced instead of the ending of the name of the parent alkane. The longest carbon chain should be numbered in a way that gives the double bond the lower number. Then the compound should be named using the first number assigned to the double bond. The names of the substituents should be written first in the alphabetic order with their position on the chain.

Answer 8

Interpretation Introduction

(b)

Interpretation:

The IUPAC name for the following alkene should be determined:

Concept Introduction:

Alkenes are named in the same way as alkanes, but the alkenes are identified by the suffix −ene, replaced instead of the ending of the name of the parent alkane. The longest carbon chain should be numbered in a way that gives the double bond the lower number. Then the compound should be named using the first number assigned to the double bond. The names of the substituents should be written first in the alphabetic order with their position on the chain.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The IUPAC name for the following alkene should be determined:

Concept Introduction:

Alkenes are named in the same way as alkanes, but the alkenes are identified by the suffix −ene, replaced instead of the ending of the name of the parent alkane. The longest carbon chain should be numbered in a way that gives the double bond the lower number. Then the compound should be named using the first number assigned to the double bond. The names of the substituents should be written first in the alphabetic order with their position on the chain.

Answer 10

Expert Solution & Answer

Answer 11

Expert Solution & Answer

Answer 12

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 13

Ch. 13.1 - Convert each condensed structure to a complete...Ch. 13.1 - Prob. 13.1P Ch. 13.1 - Complete the structure of zingiberene, a component...Ch. 13.2 - Prob. 13.2PP Ch. 13.2 - Prob. 13.3P Ch. 13.2 - Prob. 13.3PP Ch. 13.2 - Prob. 13.4PP Ch. 13.3 - Prob. 13.5PP Ch. 13.3 - Prob. 13.4P Ch. 13.3 - Prob. 13.6PP

Solution Summary: The author explains that the IUPAC name for the following alkene is 4,5-dimethyl-1-octene.

Concept explainers

Videos

Want to see the full answer?

Chapter 13 Solutions