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EBK ORGANIC CHEMISTRY AS A SECOND LANGU
4th Edition
ISBN: 9781119234722
Author: Klein
Publisher: JOHN WILEY+SONS,INC.-CONSIGNMENT
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Question
Chapter 1.2, Problem 1.6P
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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Students have asked these similar questions
Blocking 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 image **NOTE: The compound on the left is the starting point, and the compound on the right is the final product. Please show the steps in between to get from start to final, please. These are not two different compounds that need to be worked.
I dont understand this.
Can you please explain this prooblem to me, show me how the conjugation is added, did I add them in the correct places and if so please show me. Thanks!
Chapter 1 Solutions
EBK ORGANIC CHEMISTRY AS A SECOND LANGU
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
- Basic strength of organic bases.arrow_forwardNucleophilic Aromatic Substitution: What is the product of the reaction? What is the name of the intermediate complex? *See imagearrow_forwardPredict the final product. If 2 products are made, list which should be “major” and “minor” *see attachedarrow_forward
- 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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