ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.)
4th Edition
ISBN: 9781119761068
Author: Klein
Publisher: WILEY
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Question
Chapter 1.2, Problem 1.3P
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.
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Chapter 1 Solutions
ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.)
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
- Draw structures corresponding to the following names and give IUPAC names for the following compounds: (8 Point) a) b) c) CH3 CH2CH3 CH3CHCH2CH2CH CH3 C=C H3C H H2C=C=CHCH3 d) CI e) (3E,5Z)-2,6-Dimethyl-1,3,5,7-octatetraene f) (Z)-4-bromo-3-methyl-3-penten-1-yne g) cis-1-Bromo-2-ethylcyclopentane h) (5R)-4,4,5-trichloro-3,3-dimethyldecanearrow_forwardNonearrow_forwardReview: Design a total total synthesis synthesis of the following compound using methyloxacyclopropane and any other necessary reagents.arrow_forward
- Nonearrow_forwardDraw a Newman projection from carbon 3 to carbon 2 in the highest energy conformation for the following molecule. What is this conformation called? What kind of strain is present? Brarrow_forwardWhich of the following dienophiles is most reactive in a Diels-Alder reaction: Please explain why the correct answer to this question is option 5. Please provide a detailed explanation.arrow_forward
- Which of the following would you expect to be aromatic? Please provide a detailed explanation.arrow_forwardDraw the enantiomer and diastereomers of the following molecule. Label each type of stereoisomers. Label each chiral center as R or S. HOarrow_forwardWhich diene and dienophile would you choose to synthesize the following compound? Please provide a detailed explanation. Please include a drawing showing the mechanism of the synthesis. Please also explain why it is the correct diene and dienophile.arrow_forward
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