EBK GET READY FOR ORGANIC CHEMISTRY
EBK GET READY FOR ORGANIC CHEMISTRY
2nd Edition
ISBN: 9780321787989
Author: KARTY
Publisher: PEARSON CO
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Chapter A, Problem A.9P
Interpretation Introduction

Interpretation:

The IUPAC name of the molecule shown is to be written.

Concept introduction:

The root name of an alkane is determined on the basis of the longest chain of carbons. If the compound also contains a ring with more carbon atoms, then the root name is determined on the basis of number of the ring carbons, as a cycloalkane. If there are multiple substituents on the ring, the ring carbon with the greatest number of substituents is numbered 1. The rest of the ring carbons are then numbered so that the next substituent gets the lowest number. The substituents are named alphabetically. Their positions are indicated by numbers preceding the names. The numbers and names of substituents are separated by dashes. If the same substituent occurs more than once, the number is indicated by a prefix di-, tri- etc., with the positions of both indicated by appropriate numbers.

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PLEASE READ!!! I DONT WANT EXAMPLES, I DONT WANT WORDS OR PARAGRAPHS FOR THE MECHANISM!!! THANKS First image: QUESTION 6. I have to show, with ARROWS and STRUCTURES, the mechanism of the reaction at the bottom. Also I have to show by mecanism why the reaction wouldn't work if the alcohol was primary. I also tried to draw the mechanism, tell me what to change. Please note that its an AMIDE thats formed not an AMINE the nitrogen has ONE hydrogen and one Phenyl-C-Phenyl. I already asked for this mechanism and got as a final product ...-NH2 not whats shown on the picture, thank you Ths second part. QUESTION 3. I just need a way to synthesize the lactone A, I already started please continue from where I left it  Second image: I simply need the products, substrates or reagents, thank you
Indicate how to prepare a 10% sodium hydroxide (NaOH) solution to a slightly alkaline pH.
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Nomenclature: Crash Course Chemistry #44; Author: CrashCourse;https://www.youtube.com/watch?v=U7wavimfNFE;License: Standard YouTube License, CC-BY