Connect 1-Semester Access Card for General, Organic, & Biological Chemistry
Connect 1-Semester Access Card for General, Organic, & Biological Chemistry
3rd Edition
ISBN: 9781259815072
Author: Janice Gorzynski Smith Dr.
Publisher: McGraw-Hill Education
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Chapter 13.2, Problem 13.4P
Interpretation Introduction

(a)

Interpretation:

The IUPAC name for the following alkene should be determined:

  Connect 1-Semester Access Card for General, Organic, & Biological Chemistry, Chapter 13.2, Problem 13.4P , additional homework tip  1

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:

  Connect 1-Semester Access Card for General, Organic, & Biological Chemistry, Chapter 13.2, Problem 13.4P , additional homework tip  2

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

(c)

Interpretation:

The IUPAC name for the following alkene should be determined:

  Connect 1-Semester Access Card for General, Organic, & Biological Chemistry, Chapter 13.2, Problem 13.4P , additional homework tip  3

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

(d)

Interpretation:

The IUPAC name for the following alkene should be determined:

  Connect 1-Semester Access Card for General, Organic, & Biological Chemistry, Chapter 13.2, Problem 13.4P , additional homework tip  4

Concept Introduction:

In the nomenclature of cycloalkenes, the double bond is always located between C-1 and C-2. And 1 is not mentioned in the name. the ring is then numbered in a way that the first substituent getting the lowest number.

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Name each alkyne. a. CH=C-CH-CH3 CH3 b. CH3-C=C-CH-CH-CH,-CH, CH3 CH3 c. CHEC-C-CH,-CH3 CH2 ČH, CH3 d. CH;-C=C-CH-C-CH, CH2 CH3 ČH3

Chapter 13 Solutions

Connect 1-Semester Access Card for General, Organic, & Biological Chemistry

Ch. 13.3 - Prob. 13.11PCh. 13.3 - Prob. 13.12PCh. 13.3 - Prob. 13.13PCh. 13.4 - Prob. 13.14PCh. 13.6 - Prob. 13.15PCh. 13.6 - Prob. 13.16PCh. 13.6 - Prob. 13.17PCh. 13.6 - Prob. 13.18PCh. 13.6 - Prob. 13.19PCh. 13.7 - Prob. 13.20PCh. 13.8 - Prob. 13.21PCh. 13.8 - Prob. 13.22PCh. 13.10 - Give the IUPAC name of each compound. Ch. 13.10 - Prob. 13.24PCh. 13.11 - Prob. 13.25PCh. 13.12 - Prob. 13.26PCh. 13.13 - Prob. 13.27PCh. 13.13 - Prob. 13.28PCh. 13 - Anethole, the major constituent of anise oil, is...Ch. 13 - Prob. 13.30PCh. 13 - What is the molecular formula for a hydrocarbon...Ch. 13 - Prob. 13.32PCh. 13 - Prob. 13.33PCh. 13 - Prob. 13.34PCh. 13 - Prob. 13.35PCh. 13 - Prob. 13.36PCh. 13 - Give the IUPAC name for each molecule depicted in...Ch. 13 - Give the IUPAC name for each molecule depicted in...Ch. 13 - Give the IUPAC name for each compound. a....Ch. 13 - Give the IUPAC name for each compound. d....Ch. 13 - Prob. 13.41PCh. 13 - Prob. 13.42PCh. 13 - Give the structure corresponding to each IUPAC...Ch. 13 - Prob. 13.44PCh. 13 - Each of the following IUPAC names is incorrect....Ch. 13 - Each of the following IUPAC names is incorrect....Ch. 13 - Prob. 13.47PCh. 13 - Prob. 13.48PCh. 13 - Prob. 13.49PCh. 13 - Label the carbon-carbon double bond as cis or...Ch. 13 - Prob. 13.51PCh. 13 - Prob. 13.52PCh. 13 - Prob. 13.53PCh. 13 - Prob. 13.54PCh. 13 - Prob. 13.55PCh. 13 - Prob. 13.56PCh. 13 - Prob. 13.57PCh. 13 - Prob. 13.58PCh. 13 - Prob. 13.59PCh. 13 - Prob. 13.60PCh. 13 - What alkyd halide is formed when each alkene is...Ch. 13 - Prob. 13.62PCh. 13 - Prob. 13.63PCh. 13 - Prob. 13.64PCh. 13 - What alkene is needed as a starting material to...Ch. 13 - Prob. 13.66PCh. 13 - Prob. 13.67PCh. 13 - Prob. 13.68PCh. 13 - Prob. 13.69PCh. 13 - Prob. 13.70PCh. 13 - Prob. 13.71PCh. 13 - Prob. 13.72PCh. 13 - Prob. 13.73PCh. 13 - Prob. 13.74PCh. 13 - Prob. 13.75PCh. 13 - Prob. 13.76PCh. 13 - Prob. 13.77PCh. 13 - Prob. 13.78PCh. 13 - Prob. 13.79PCh. 13 - Prob. 13.80PCh. 13 - Prob. 13.81PCh. 13 - Are o-bromochlorobenzene and m-bromochlorobenzene...Ch. 13 - Give the structure corresponding to each IUPAC...Ch. 13 - Give the structure corresponding to each IUPAC...Ch. 13 - Prob. 13.85PCh. 13 - Prob. 13.86PCh. 13 - Prob. 13.87PCh. 13 - Prob. 13.88PCh. 13 - Prob. 13.89PCh. 13 - Prob. 13.90PCh. 13 - Prob. 13.91PCh. 13 - Prob. 13.92PCh. 13 - Prob. 13.93PCh. 13 - Eleostearic acid is an unsaturated fatty acid...Ch. 13 - Prob. 13.95PCh. 13 - Prob. 13.96PCh. 13 - Prob. 13.97PCh. 13 - Prob. 13.98PCh. 13 - Prob. 13.99PCh. 13 - Prob. 13.100PCh. 13 - Prob. 13.101PCh. 13 - Prob. 13.102PCh. 13 - Answer the following questions about compound A,...Ch. 13 - Prob. 13.104PCh. 13 - Prob. 13.105PCh. 13 - Prob. 13.106PCh. 13 - Prob. 13.107CPCh. 13 - Prob. 13.108CP
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