ORGANIC CHEMISTRY
ORGANIC CHEMISTRY
6th Edition
ISBN: 9781266633973
Author: SMITH
Publisher: MCG
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Chapter 10, Problem 32P

Give the IUPAC name for each compound.

a.Chapter 10, Problem 32P, Give the IUPAC name for each compound. a.b. , example  1 b. Chapter 10, Problem 32P, Give the IUPAC name for each compound. a.b. , example  2

Expert Solution
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Interpretation Introduction

(a)

Interpretation: The IUPAC name for the given compound is to be stated.

Concept introduction: The systematic naming of organic compound is given by IUPAC. The naming of organic compound is done such that the structure of organic compound is correctly interpreted from the name.

Rules for writing IUPAC name from structural formula are

1. First identify the longest carbon chain.

2. The next step is to identify the groups attached to the longest chain.

3. Identify the position, location, and number of the substituent bonded to the carbon chain.

4. Use prefix di, tri, tetra if same type of substituent is present.

5. Name the substituents in alphabetical order.

Answer to Problem 32P

The IUPAC name for the given compound is 3,5dimethylhex2ene.

Explanation of Solution

The given compound is,

ORGANIC CHEMISTRY, Chapter 10, Problem 32P , additional homework tip  1

Figure 1

The ball and stick model of the compound is given. The black color ball represents the carbon atom and white color ball represent the hydrogen atom.

The numbering of carbon atoms present in the longest carbon chain is shown below.

ORGANIC CHEMISTRY, Chapter 10, Problem 32P , additional homework tip  2

Figure 2

The longest carbon chain has six carbon atoms. The root word used for six carbon atoms is hex and the suffix used for C=C linkage is –ene. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order. One methyl substituents is attached to the third and fifth carbon atom. The double bond is present between second and third carbon atom. Thus, the IUPAC name of the given structure is 3,5dimethylhex2ene.

Conclusion

The IUPAC name for the given compound is 3,5dimethylhex2ene.

Expert Solution
Check Mark
Interpretation Introduction

(b)

Interpretation: The IUPAC name for the given compound is to be stated.

Concept introduction: The systematic naming of organic compound is given by IUPAC. The naming of organic compound is done such that the structure of organic compound is correctly interpreted from the name.

Rules for writing IUPAC name from structural formula are

1. First identify the longest carbon chain.

2. The next step is to identify the groups attached to the longest chain.

3. Identify the position, location, and number of the substituent bonded to the carbon chain.

4. Use prefix di, tri, tetra if same type of substituent is present.

5. Name the substituents in alphabetical order.

Answer to Problem 32P

The IUPAC name for the given compound is 1(sec-butyl)2methylcyclopent1ene.

Explanation of Solution

The given compound is,

ORGANIC CHEMISTRY, Chapter 10, Problem 32P , additional homework tip  3

Figure 3

The ball and stick model of the compound is given. The black color ball represents the carbon atom and white color ball represent the hydrogen atom.

The numbering of carbon atoms present in the longest carbon chain is shown below.

ORGANIC CHEMISTRY, Chapter 10, Problem 32P , additional homework tip  4

Figure 4

The longest carbon chain has five carbon atoms. The root word used for five carbon atoms is pent and the suffix used for C=C linkage is –ene. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order. One methyl substituents is attached to the second carbon atom and one secondary butyl substituents is attached to the first carbon atom. The double bond is present between first and second carbon atom. Thus, the IUPAC name of the given structure is 1(sec-butyl)2methylcyclopent1ene.

Conclusion

The IUPAC name for the given compound is 1(sec-butyl)2methylcyclopent1ene.

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Chapter 10 Solutions

ORGANIC CHEMISTRY

Ch. 10.10 - Prob. 16PCh. 10.10 - Prob. 17PCh. 10.10 - Addition of HBr to which of the following alkenes...Ch. 10.11 - Problem 10.19 Draw the products, including...Ch. 10.11 - Prob. 20PCh. 10.12 - Problem 10.21 What two alkenes give rise to each...Ch. 10.12 - Prob. 22PCh. 10.13 - Problem 10.23 Draw the products of each reaction,...Ch. 10.14 - Problem 10.24 Draw all stereoisomers formed in...Ch. 10.15 - Prob. 25PCh. 10.16 - Problem 10.26 What alkylborane is formed from...Ch. 10.16 - Draw the products formed when each alkene is...Ch. 10.16 - What alkene can be used to prepare each alcohol as...Ch. 10.16 - Prob. 29PCh. 10.17 - Draw the products of each reaction using the two...Ch. 10.18 - Problem 10.31 Devise a synthesis of each compound...Ch. 10 - Give the IUPAC name for each compound. a.b.Ch. 10 - a Label the carbon-carbon double bond in A as E or...Ch. 10 - Prob. 34PCh. 10 - 10.35 Calculate the number of degrees of...Ch. 10 - Prob. 36PCh. 10 - Label the alkene in each drug as E or Z....Ch. 10 - Give the IUPAC name for each compound. a. c. e. b....Ch. 10 - Prob. 39PCh. 10 - 10.40 (a) Draw all possible stereoisomers of, and...Ch. 10 - Prob. 41PCh. 10 - 10.42 Now that you have learned how to name...Ch. 10 - Prob. 43PCh. 10 - Prob. 44PCh. 10 - Prob. 45PCh. 10 - Draw the products formed when (CH3)2C=CH2 is...Ch. 10 - What alkene can be used to prepare each alkyl...Ch. 10 - Prob. 48PCh. 10 - Draw the constitutional isomer formed in each...Ch. 10 - Prob. 50PCh. 10 - Draw all stereoisomers formed in each reaction. a....Ch. 10 - Draw the products of each reaction, including...Ch. 10 - Prob. 53PCh. 10 - Draw a stepwise mechanism that shows how all three...Ch. 10 - Less stable alkenes can be isomerized to more...Ch. 10 - Prob. 60PCh. 10 - Prob. 61PCh. 10 - Bromoetherification, the addition of the elements...Ch. 10 - Devise a synthesis of each product from the given...Ch. 10 - 10.65 Draw a synthesis of each compound from...
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