O Nothing. It is correctly named and the steps are correct. Step 1: The parent chain has 10 carbon atoms and should be decane. Step 2: The parent chain is numbered backwards (carbon 1 should be at the bottom, not the top). O Step 3: The substituents are not methyl substituents, they are ethyl substituents.

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter17: Alcohols And Phenols
Section17.SE: Something Extra
Problem 69AP: As a rule, axial alcohols oxidize somewhat faster than equatorial alcohols. Which would you expect...
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What is wrong with the steps or the name of this compound?

CH3
4
3
H₂C ·C CH₂
5 CH₂ CH₂
this end closest to
first branch, so it's
STEP 1: 8C-octane
1
2
1
CH₂-CH3) STEP 2: number Parent
H₂C-CH₂
7
STEP 3: 4-methyl
4-methy!
STEP 4:
4,4-dimethyloctane
Nothing. It is correctly named and the steps are correct.
Step 1: The parent chain has 10 carbon atoms and should be decane.
Step 2: The parent chain is numbered backwards (carbon 1 should be at the
bottom, not the top).
Step 3: The substituents are not methyl substituents, they are ethyl
substituents.
Transcribed Image Text:CH3 4 3 H₂C ·C CH₂ 5 CH₂ CH₂ this end closest to first branch, so it's STEP 1: 8C-octane 1 2 1 CH₂-CH3) STEP 2: number Parent H₂C-CH₂ 7 STEP 3: 4-methyl 4-methy! STEP 4: 4,4-dimethyloctane Nothing. It is correctly named and the steps are correct. Step 1: The parent chain has 10 carbon atoms and should be decane. Step 2: The parent chain is numbered backwards (carbon 1 should be at the bottom, not the top). Step 3: The substituents are not methyl substituents, they are ethyl substituents.
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