Organic Chemistry
Organic Chemistry
4th Edition
ISBN: 9780073402772
Author: Janice G. Smith
Publisher: MCG
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Chapter 11, Problem 11.1P

Draw structures for the three alkynes having molecular formula C5H8 and classify each as an internal or terminal alkyne.

Expert Solution
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Interpretation Introduction

Interpretation: The three alkynes having molecular formula C5H8 is to be drawn and each is to be classified as an internal or terminal alkyne.

Concept Introduction: Alkynes are an unsaturated hydrocarbon having at least one carbon-carbon triple bond. The general formula of alkynes are CnH2n-2. The simplest hydrocarbon of alkyne family is acetylene having two carbon atom. Alkynes can be divided into the following two categories based on the position of triple bond; 1) internal alkyne 2) terminal alkyne. In internal alkynes there are no hydrogen atoms bonded to triply bonded carbon atoms. In terminal alkynes there is at least one hydrogen atom bonded to a triply bonded carbon atom.

Answer to Problem 11.1P

the internal and terminal alkynes of molecular formula C5H8 are as follows;

Organic Chemistry, Chapter 11, Problem 11.1P

Explanation of Solution

In pent-1-yne and 3-methyl but-1-yne the triple bond is at the terminal side of carbon having one -C-H group. Thus, they are called as terminal alkynes. In case of pent-2-yne the triple bond is in the middle of carbon having no free -C-H group. Thus, it is called as internal alkyne.

Conclusion

Thus, the alkynes of formula C5H is drawn and named as an internal alkyne or terminal alkyne.

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Chapter 11 Solutions

Organic Chemistry

Ch. 11 - Explain the following result. Although alkenes...Ch. 11 - Problem 11.11 Draw the keto tautomer of each...Ch. 11 - Prob. 11.13PCh. 11 - a Draw two different enol tautomers of...Ch. 11 - Prob. 11.15PCh. 11 - Prob. 11.16PCh. 11 - Prob. 11.17PCh. 11 - Problem. 11.17 Show how , and can be used to...Ch. 11 - Prob. 11.19PCh. 11 - Draw the products of each reaction. a. b.Ch. 11 - Prob. 11.21PCh. 11 - Problem 11.21 Use retrosynthetic analysis to show...Ch. 11 - Prob. 11.23PCh. 11 - Give the IUPAC name for each compound. a. b.Ch. 11 - Prob. 11.25PCh. 11 - 11.25 Answer the following questions about...Ch. 11 - Prob. 11.27PCh. 11 - Give the IUPAC name for each alkyne.Ch. 11 - Prob. 11.29PCh. 11 - Which of the following pairs of compounds...Ch. 11 - Prob. 11.31PCh. 11 - 11.30 How is each compound related to A? Choose...Ch. 11 - Prob. 11.33PCh. 11 - Prob. 11.34PCh. 11 - Prob. 11.35PCh. 11 - 11.33 Draw the products formed when is treated...Ch. 11 - Draw the products formed when 3-hexyne is treated...Ch. 11 - Prob. 11.38PCh. 11 - Prob. 11.39PCh. 11 - What alkynes give each of the following ketones as...Ch. 11 - Prob. 11.41PCh. 11 - 11.37 What alkyne gives each compound as the only...Ch. 11 - Prob. 11.43PCh. 11 - Draw the structure of compounds A-E in the...Ch. 11 - Prob. 11.45PCh. 11 - Prob. 11.46PCh. 11 - 11.42 What reactions are needed to convert alcohol...Ch. 11 - Prob. 11.48PCh. 11 - Prob. 11.49PCh. 11 - 11.45 Explain the following statement. Although ...Ch. 11 - Draw a stepwise mechanism for the following...Ch. 11 - Prob. 11.52PCh. 11 - Prob. 11.53PCh. 11 - Prob. 11.54PCh. 11 - Prob. 11.55PCh. 11 - Synthesize each compound from acetylene. You may...Ch. 11 - Prob. 11.57PCh. 11 - Prob. 11.58PCh. 11 - 11.55 Devise a synthesis of the ketone, , from ...Ch. 11 - 11.56 Devise a synthesis of each compound using ...Ch. 11 - Prob. 11.61PCh. 11 - Prob. 11.62PCh. 11 - 11.60 Draw a stepwise mechanism for the following...Ch. 11 - Draw a stepwise mechanism for the following...Ch. 11 - Prob. 11.65PCh. 11 - Write a stepwise mechanism for each of the...Ch. 11 - Prob. 11.67PCh. 11 - 11.65 Explain why an optically active solution of ...
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