List each substituent on the main chain of this organic molecule on a separate row of the table below:CH3 CH2 CH2CH3-CH2-CH-CH-CH-CH2-CH2-CH2-CH3CH3 CH3-CH-CH3Your answer for the name column should be just one word. In the location column, write the number of the carbon where the substituent is attached to the mainchain.You can add more rows to the table if you need them.nameAdd Rowlocation06GAr

Step 1: Rule for IUPAC NamingFind the highest priority functional group.Determine and name the…

Answered: List each substituent on the main chain…

Chemistry for Today: General, Organic, and Biochemistry

9th Edition

ISBN:9781305960060

Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Publisher:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Chapter14: Aldehydes And Ketones

Section: Chapter Questions

Problem 14.53E

See similar textbooks

Similar questions

Give the common name for 0 || CH3 CH3-C-N-CH2 —CH₂ —CH3 Spell out the common name of the compound. Submit Request Answer Part F Give the IUPAC name for CH2-CH3 N-CH2-CH3 Spell out the IUPAC name of the compound.
O HYDROCARBONS Naming branched alkanes Name the following organic compounds: CH3 | Explanation compound CH3 I CH₂-CH₂-CH-CH₂ CH₂ - CH₂ - CH3 | CH3-CH₂-C- CH₂ - CH₂ - CH3 | CH3 - CH₂ - CH₂ Check CH3 — CH₂-CH-CH₂ - CH₂ name I 0 X Ś Ⓒ2022 McGraw Hill
List the name and position for each substituent in this organic molecule on a separate row of the table below: CH3 Q-CH₂-CH3 CH3–CH–CH2–CH-CH=CH2–CH2–CH3 CH₂-CH₂-CH3 Your answer for the name column should be just one word. In the position column, write the number of the carbon where the substituent is attached to the parent chain (which has been highlighted for you). Note for advanced students: You may assume that the parent chain is numbered from left-to-right in this molecule. You can add more rows to the table if you need them. name Add Row position 0 X
c7
Analyze the structure of 4‑sec‑butyl-5-ethyl-3-methyloctane. Identify the number of ethyl and methyl groups in the compound. Note that these groups are not necessarily confined to those specifically mentioned in the name.
Write the systematic (IUPAC) name for each of the following organic molecules: structure CH3 CH2 CH3-N-CH2-CH2-CH3 CH3-CH2-CH- -CH-CH2-CH3 NH CH2 CH₂ CH3 CH3-CH2-CH2-CH2-CH2-CH2-CH2-N-CH2-CH3 CH₂ CH3 name olo
Payalben
Pick the best IUPAC name for the following molecule: Cl- OH O1-chloro-6-fluorocyclohexan-3-ol 1-chloro-2-fluorocyclohexanone O 3-chloro-4-fluorocyclohexan-1-ol O 1-chloro-2-fluorocyclohexan-5-ol
find out correct and incorrect IUPAC name and give reason behind it!
Write the systematic (IUPAC) name for each of the following organic molecules: structure OH CH3 C CH3 CH3 CH₂ CH3 CH3CH2C–CH2–CH2C−CH2CH3 CH3 CH2 OH CH3 CH3-CH₂ OH CH₂ CH3 CH3—CH,—CH–CH2–CH2–CH–CH2–CH-CH2CH3 name
What is the IUPAC name of the following molecule
2. The molecules shown below are four terpineol isomers. They are isolated from plants and have distinct aromas. For example, a -terpineol is a common perfume ingredient and smells similar to lilacs. HO a-terpineol ß-terpineol y-terpineol 4-terpineol A) How many of each of the different types of carbon are present in 4-terpineol. Do not consider carbons attached to heteroatoms or participating in pi bonds. i. Primary ii. Secondary iii. Tertiary iv. Quaternary B) Terpineols contain tertiary alcohols. While quaternary carbons exist, quaternary alcohols do not. Explain why a quaternary alcohol is not feasible. C) Is it necessary to use E/Z designations for any of these molecules? If so, provide the proper designation for each relevant molecule. If not, briefly explain why it isn't needed. e. Draw a structural isomer of terpineol that meet the following criteria. You should draw one unique structure for each set. You must draw each molecule twice, once as a skeletal structure and once as a…

SEE MORE QUESTIONS

Recommended textbooks for you

Chemistry for Today: General, Organic, and Bioche…

Chemistry

ISBN:

9781305960060

Author:

Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Publisher:

Cengage Learning

Introductory Chemistry: A Foundation

Chemistry

ISBN:

9781337399425

Author:

Steven S. Zumdahl, Donald J. DeCoste

Publisher:

Cengage Learning

Chemistry for Today: General, Organic, and Bioche…

Chemistry

ISBN:

9781305960060

Author:

Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Publisher:

Cengage Learning

Introductory Chemistry: A Foundation

Chemistry

ISBN:

9781337399425

Author:

Steven S. Zumdahl, Donald J. DeCoste

Publisher:

Cengage Learning

SEE MORE TEXTBOOKS