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Organic Chemistry As a Second Language: Second Semester Topics
4th Edition
ISBN: 9781119110651
Author: David R. Klein
Publisher: WILEY
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Question
Chapter 1.2, Problem 1.2P
Interpretation Introduction
Interpretation:
A systematic name for the given compound has to be provided.
Concept Introduction:
Nomenclature of
- The parent is benzene ring.
Functional groups attached to it other than hydrogens are called substituents. The name of substituent must be placed before the name of the compound as a prefix in any substituted hydrocarbon.Ex.
- The numerical prefixes such as di, tri, and tetra must be included in the nomenclature if more than one similar substituents are attached to the benzene ring.
Ex.
- If different substituent groups are attached to the benzene ring, the no. one position is determined by the parent. So the first step is to choose a suitable parent. Then the locants are assigned in a manner that gives the lower possible number to the next substituent.
Ex.
- For disubstituted benzenes, prefixes such as ortho, meta and para should be used.
Ex.
Expert Solution & Answer
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Chapter 1 Solutions
Organic Chemistry As a Second Language: Second Semester Topics
Ch. 1.2 - Prob. 1.2PCh. 1.2 - Prob. 1.3PCh. 1.2 - Prob. 1.4PCh. 1.2 - Prob. 1.5PCh. 1.2 - Prob. 1.6PCh. 1.3 - Characterize each of the following structures as...Ch. 1.3 - Characterize each of the following structures as...Ch. 1.3 - Characterize each of the following structures as...Ch. 1.3 - Characterize each of the following structures as...Ch. 1.3 - Characterize each of the following structures as...
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Similar questions
- Nucleophilic Aromatic Substitution: What is the product of the reaction? *see imagearrow_forwardShow the correct sequence to connect the reagent to product. * see imagearrow_forwardThe answer here says that F and K have a singlet and a doublet. The singlet and doublet are referring to the H's 1 carbon away from the carbon attached to the OH. Why don't the H's two carbons away, the ones on the cyclohexane ring, cause more peaks on the signal?arrow_forward
- Draw the Birch Reduction for this aromatic compound and include electron withdrawing groups and electron donating groups. *See attachedarrow_forwardShow the correct sequence to connect the reagent to product. * see imagearrow_forwardBlocking Group are use to put 2 large sterically repulsive group ortho. Show the correct sequence toconnect the reagent to product with the highest yield possible. * see imagearrow_forward
- Elimination-Addition: What molecule was determined to be an intermediate based on a “trapping experiment”? *please solve and see imagearrow_forwardShow the correct sequence to connect the reagent to product. * see imagearrow_forwardPredict the final product. If 2 products are made, list which should be “major” and “minor”. **see attachedarrow_forward
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