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–CHCH–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 0 position 0 X S

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–CHCH–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 0 position 0 X S

Chemistry: An Atoms First Approach

2nd Edition

ISBN:9781305079243

Author:Steven S. Zumdahl, Susan A. Zumdahl

Publisher:Steven S. Zumdahl, Susan A. Zumdahl

Chapter21: Organic And Biological Molecules

Section: Chapter Questions

Problem 1Q

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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
Classify each of the molecules according to its functional group. H-С- СН2— СHз HocLo-c-Ct, НзС—С—0—сH2—CНз НзС—CН2—Сн H3C-NH-CH2-CH3 H3C-Ĉ-CH,-CH3 %3D НаС—С—н Br нас НзС—сн—сн2—СHз Нзс—CН2—СH2—C-он |3| Нзс—CH2—С—NH2 НзС—CН2—0—CHз Answer Bank ether ester ketone halide amine alcohol aldehyde carboxylic acid amide
A carbon skeleton for cyclohexane is shown below. Where on that skeleton would the substituents be located in 4-chloro-1-ethyl-2-methylcyclohexane? Identify the appropriate carbon atoms by selecting each atom individually on the canvas and assigning them a map number of [1], [2], or [4] until all atoms are mapped.
= ALEKS O ORGANIC FUNCTIONAL GROUPS Naming and drawing unsubstituted esters Write the systematic name of each organic molecule: structure O CH3-0-C-CH3 O CH3–CH2–CH2–CH2-C−O−CH2–CH, CH 0=0 CH3-CH₂-CH₂-C-0-CH3 A ALEKS-Kimberly Cedillos - Learn name 0 0 G Write the systematic name of each organic molec 0/5 || Kimberl
______ is an organic compound characterized by the presence of the -COOH functional group. The name of a ketone that has 6 carbon atom where the =O (oxo) group is attached to the 3rd carbon atom (C6C5C4C3C2C1) and a CH3 and Br substituents attached at the 4th and 5th carbon atom respectively is _____. An ether has the following structural formula: CH3-CH2-O-CH2-CH2-CH3. The IUPAC name is _____.
List the name and position for each substituent in this organic molecule on a separate row of the table below: CH3CH2CH2Ọ CH3 CH3–CH2–CH–CH2–CH–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 Ś
Organic Functional Groups Naming and drawing carboxylic acids Write the systematic name of each organic molecule: CH₂ HO-C-CH-CHCH,—CH,—CH,—0 O --- CH₂ structure CH₂ CI-CH₂-CH-CH₂-C-OH i O=C 010 - HỌ—CCH,CH, OH CAL pen JANO name 0 10 0 -
Write the common (not systematic) name of each organic molecule. CH3 structure CH3 CH₂CH3 -CH-N-CH-CH3 I CH3 CH3 CH3 CH₂-N-CH₂-CH3 CH3 CH3 -CH₂ - CH₂-N-CH₂-CH₂ - CH3 name
Write the systematic (IUPAC) name for each of the following organic molecules: structure CH3CH2NH—CH2 CH2CH2CH2CH2CH3 CH3CH2 CH2 CH2 CH2N-CH2 CH2 CH3 CH₂ CH3 CH3 CH2 CH2NHCH2CH3 name 0 0 0
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…
The name of a ketone that has 6 carbon atom where the =O (oxo) group is attached to the 3rd carbon atom (C6C5C4C3C2C1) and a CH3 and Br substituents attached at the 4th and 5th carbon atom respectively is
These two compounds represent the same organic compound. CH3 CH3-CH-CH-CH2-CH2-CH3 CH2 CH3