ORGANIC CHEMISTRY MASTERINGCHEM ACCESS
9th Edition
ISBN: 9780137249442
Author: Wade
Publisher: INTER PEAR
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Question
Chapter 10.12, Problem 10.28P
(a)
Interpretation Introduction
To determine: The IUPAC name for the given compound.
Interpretation: The IUPAC name for the given compound is to be stated.
Concept introduction: The IUPAC naming of the compounds are based on the following rules given below.
- 1. The longest carbon chain that contains the carbon atom bearing the main
functional group is selected as the root chain. - 2. The longest carbon chain is numbered starting at the end nearest to the main functional group and number is used to show the position of atom bearing the main functional group
- 3. All the substituents are named and numbers are given to their position in the longest carbon chain.
(b)
Interpretation Introduction
To determine: The IUPAC name for the given compound.
Interpretation: The IUPAC name for the given compound is to be stated.
Concept introduction: The IUPAC naming of the compounds are based on the following rules given below.
- 1. The longest carbon chain that contains the carbon atom bearing the main functional group is selected as the root chain.
- 2. The longest carbon chain is numbered starting at the end nearest to the main functional group and number is used to show the position of atom bearing the main functional group
- 3. All the substituents are named and numbers are given to their position in the longest carbon chain.
(c)
Interpretation Introduction
To determine: The IUPAC name for the given compound.
Interpretation: The IUPAC name for the given compound is to be stated.
Concept introduction: The IUPAC naming of the compounds are based on the following rules given below.
- 1. The longest carbon chain that contains the carbon atom bearing the main functional group is selected as the root chain.
- 2. The longest carbon chain is numbered starting at the end nearest to the main functional group and number is used to show the position of atom bearing the main functional group
- 3. All the substituents are named and numbers are given to their position in the longest carbon chain.
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Provide IUPAC names for the following compounds
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Chapter 10 Solutions
ORGANIC CHEMISTRY MASTERINGCHEM ACCESS
Ch. 10.3A - Prob. 10.1PCh. 10.3B - Give both the IUPAC name and the common name for...Ch. 10.3B - Prob. 10.3PCh. 10.3C - Give a systematic (IUPAC) name for each diol. a....Ch. 10.4B - Predict which member of each pair will be more...Ch. 10.4B - Dimethylamine (CH3)2NH, has a molecular weight of...Ch. 10.6A - Prob. 10.7PCh. 10.6A - Prob. 10.8PCh. 10.6C - A nitro group (NO2) effectively stabilizes a...Ch. 10.6C - Prob. 10.10P
Ch. 10.8B - Prob. 10.11PCh. 10.8B - Prob. 10.12PCh. 10.9A - Prob. 10.13PCh. 10.9B - Prob. 10.14PCh. 10.9C - Show how you would synthesize each tertiary...Ch. 10.9D - Prob. 10.16PCh. 10.9D - Show how you would add Grignard reagents to acid...Ch. 10.9D - A formate ester, such as ethyl formate, reacts...Ch. 10.9E - Prob. 10.19PCh. 10.9E - In Section9-7B, we saw how acetylide ions add to...Ch. 10.9F - Prob. 10.21PCh. 10.10A - Prob. 10.22PCh. 10.10B - Prob. 10.23PCh. 10.11B - Predict the products you would expect from the...Ch. 10.11B - Prob. 10.25PCh. 10.11B - Prob. 10.26PCh. 10.12 - Prob. 10.27PCh. 10.12 - Prob. 10.28PCh. 10.12 - Authentic skunk spray has become valuable for use...Ch. 10 - Give a systematic (IUPAC) name for each alcohol....Ch. 10 - Give systematic (IUPAC) names for the following...Ch. 10 - Draw the structures of the following compounds...Ch. 10 - Predict which member of each pair has the higher...Ch. 10 - Predict which member of each pair is more acidic,...Ch. 10 - Predict which member of each group is most soluble...Ch. 10 - Draw the organic products you would expect to...Ch. 10 - Prob. 10.37SPCh. 10 - Show how you would synthesize the following...Ch. 10 - Show how you would use Grignard syntheses to...Ch. 10 - Show how you would accomplish the following...Ch. 10 - Show how you would synthesize the following: a....Ch. 10 - Complete the following acid-base reactions. In...Ch. 10 - Prob. 10.43SPCh. 10 - Prob. 10.44SPCh. 10 - Geminal diols, or 1,1-diols, are usually unstable,...Ch. 10 - Vinyl alcohols are generally unstable, quickly...Ch. 10 - Compound A (C7H11Br) is treated with magnesium in...Ch. 10 - Prob. 10.48SPCh. 10 - Prob. 10.49SPCh. 10 - Prob. 10.50SPCh. 10 - Prob. 10.51SPCh. 10 - Prob. 10.52SPCh. 10 - Prob. 10.53SPCh. 10 - Prob. 10.54SPCh. 10 - Prob. 10.55SPCh. 10 - Prob. 10.56SPCh. 10 - Show how this 1 alcohol can be made from the...Ch. 10 - Prob. 10.58SPCh. 10 - Prob. 10.59SPCh. 10 - Prob. 10.60SP
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