EP FUND.OF GENERAL,ORG...-MOD.MASTERING
EP FUND.OF GENERAL,ORG...-MOD.MASTERING
8th Edition
ISBN: 9780134326061
Author: McMurry
Publisher: PEARSON CO
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Chapter 13.2, Problem 13.1P

(a)

Interpretation Introduction

Interpretation:

The IUPAC name of the given compound to be predicted

Concept Introduction:

IUPAC naming nomenclature:

  • Name the parent compound: Find the longest chain containing the double bond or triple bond and add the suffix ‘-ene’ or ‘-yne’ to the end of the main chain name.
  • Number the carbon atoms in the main chain so that those with multiple bonds have the lowest index numbers possible:
  • Write the full name: List the substituents in alphabetical order. Use commas to separate the numbers and the hyphen to separate number from words.  Indicate the position of double or triple bond in chain by giving the number of the first multiple-bond carbon.

(b)

Interpretation Introduction

Interpretation:

The IUPAC name of the given compound to be predicted

Concept Introduction:

IUPAC naming nomenclature:

  • Name the parent compound: Find the longest chain containing the double bond or triple bond and add the suffix ‘-ene’ or ‘-yne’ to the end of the main chain name.
  • Number the carbon atoms in the main chain so that those with multiple bonds have the lowest index numbers possible:
  • Write the full name: List the substituents in alphabetical order. Use commas to separate the numbers and the hyphen to separate number from words. Indicate the position of double or triple bond in chain by giving the number of the first multiple-bond carbon.

(c)

Interpretation Introduction

Interpretation:

The IUPAC name of the given compound to be predicted

Concept Introduction:

IUPAC naming nomenclature:

  • Name the parent compound: Find the longest chain containing the double bond or triple bond and add the suffix ‘-ene’ or ‘-yne’ to the end of the main chain name.
  • Number the carbon atoms in the main chain so that those with multiple bonds have the lowest index numbers possible:
  • Write the full name: List the substituents in alphabetical order. Use commas to separate the numbers and the hyphen to separate number from words. Indicate the position of double or triple bond in chain by giving the number of the first multiple-bond carbon.

(d)

Interpretation Introduction

Interpretation:

The IUPAC name of the given compound to be predicted

Concept Introduction:

IUPAC naming nomenclature:

  • Name the parent compound: Find the longest chain containing the double bond or triple bond and add the suffix ‘-ene’ or ‘-yne’ to the end of the main chain name.
  • Number the carbon atoms in the main chain so that those with multiple bonds have the lowest index numbers possible:
  • Write the full name: List the substituents in alphabetical order. Use commas to separate the numbers and the hyphen to separate number from words. Indicate the position of double or triple bond in chain by giving the number of the first multiple-bond carbon.

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Chapter 13 Solutions

EP FUND.OF GENERAL,ORG...-MOD.MASTERING

Ch. 13.5 - Prob. 13.3CIAPCh. 13.6 - Prob. 13.9PCh. 13.6 - Prob. 13.10PCh. 13.6 - Prob. 13.11PCh. 13.6 - Prob. 13.12PCh. 13.6 - Prob. 13.13PCh. 13.6 - Prob. 13.14KCPCh. 13.6 - Prob. 13.1MRPCh. 13.6 - Prob. 13.2MRPCh. 13.6 - Prob. 13.3MRPCh. 13.7 - Prob. 13.15PCh. 13.7 - Prob. 13.16PCh. 13.8 - Prob. 13.17PCh. 13.8 - Polychlorotrifluoroethylene (PCTFE (Kel-F)) is a...Ch. 13.9 - Prob. 13.19PCh. 13.9 - Prob. 13.20PCh. 13.9 - Prob. 13.21KCPCh. 13.10 - What products will be formed when toluene is...Ch. 13.10 - Prob. 13.23PCh. 13.10 - Prob. 13.4CIAPCh. 13.10 - Prob. 13.5CIAPCh. 13.10 - Prob. 13.6CIAPCh. 13 - Prob. 13.24UKCCh. 13 - Prob. 13.25UKCCh. 13 - Prob. 13.26UKCCh. 13 - Draw the product from reaction of the following...Ch. 13 - Prob. 13.28UKCCh. 13 - Prob. 13.29UKCCh. 13 - Prob. 13.30APCh. 13 - Prob. 13.31APCh. 13 - What family-name endings are used for alkenes,...Ch. 13 - Prob. 13.33APCh. 13 - Prob. 13.34APCh. 13 - Write structural formulas for compounds that meet...Ch. 13 - Prob. 13.36APCh. 13 - Prob. 13.37APCh. 13 - Draw structures corresponding to the following...Ch. 13 - Draw structures corresponding to the following...Ch. 13 - Seven alkynes have the formula C6H10. Draw them,...Ch. 13 - Prob. 13.41APCh. 13 - Prob. 13.42APCh. 13 - There are four different pentenes having the...Ch. 13 - Prob. 13.44APCh. 13 - Prob. 13.45APCh. 13 - Draw line structures for the following alkenes....Ch. 13 - Which compound(s) in Problem 13.43 can exist as...Ch. 13 - Prob. 13.48APCh. 13 - Prob. 13.49APCh. 13 - Which of the following pairs are isomers, and...Ch. 13 - Prob. 13.51APCh. 13 - Prob. 13.52APCh. 13 - Prob. 13.53APCh. 13 - Prob. 13.54APCh. 13 - Prob. 13.55APCh. 13 - Prob. 13.56APCh. 13 - Prob. 13.57APCh. 13 - Prob. 13.58APCh. 13 - Prob. 13.59APCh. 13 - What alkene could you use to make the following...Ch. 13 - Prob. 13.61APCh. 13 - Prob. 13.62APCh. 13 - Prob. 13.63APCh. 13 - Prob. 13.64APCh. 13 - For each of the following reagents, decide whether...Ch. 13 - Prob. 13.66APCh. 13 - Prob. 13.67APCh. 13 - Prob. 13.68APCh. 13 - Salicylic acid (o-hydroxybenzoic acid) is used as...Ch. 13 - The following names are incorrect by IUPAC rules....Ch. 13 - Prob. 13.71CPCh. 13 - Prob. 13.72CPCh. 13 - Prob. 13.73CPCh. 13 - Prob. 13.74CPCh. 13 - Menthene, a compound found in mint plants, has the...Ch. 13 - Prob. 13.76CPCh. 13 - Prob. 13.77CPCh. 13 - Two products are possible when 2-pentene is...Ch. 13 - Ocimene, a compound isolated from the herb basil,...Ch. 13 - Describe how you could prepare the following...Ch. 13 - Which of the following compounds are capable of...Ch. 13 - Prob. 13.82GPCh. 13 - Superglue is an alkene polymer made from the...Ch. 13 - Draw all possible C5H10 alkene isomers having a...
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