d) H CI Foll H CI с н говорит ОН f) CH3 ОН H3C- O-CH3 O-CH3 тон

Chemistry
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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Pls answer d-f

Determine the structural relationship between the compounds in each of the pairs that follow. They may be unrelated, identical (the same compound), constitutional isomers, diastereomers, or enantiomers. 

- Identify the optically active (chiral) compounds and any _meso_ compounds.
- Assign a configuration (R or S) to all stereocenters.
- Name all compounds so that the name reflects the structure unambiguously.

### a)
1. Left compound:
   - Structure: CHO, NH2, HO, CH2OH
   - Groups: Aldehyde, amine, hydroxyl, and primary alcohol groups

2. Right compound:
   - Structure: CH2OH, OH, H, NH2, CHO
   - Groups: Primary alcohol, hydroxyl, hydrogen, amine, and aldehyde groups.

### b)
1. Left compound:
   - Cyclohexane with wedge and dash substituents: H (wedge) and CH3 (dash)
   
2. Right compound:
   - Cyclohexane with wedge and dash substituents: CH3 (wedge) and H (dash)

### c)
1. Left compound:
   - Central carbon with four groups: H, CH3, Cl, Ph (phenyl)
   - Stereochemistry indicated by solid wedges (towards viewer) and dashed lines (away from viewer)

2. Right compound:
   - Central carbon similar to left, arranged differently: Ph, CH3, Cl, H
   - Stereochemistry indicated by solid wedges (towards viewer) and dashed lines (away from viewer)

### d)
1. Left compound:
   - Cyclic structure with Cl (wedge) and H (dash), carbonyl (C=O) present.

2. Right compound:
   - Cyclic structure with H (wedge) and Cl (dash), carbonyl (C=O) present.

### e)
1. Left compound:
   - Six-membered ring, carbonyl group, methyl branch (CH3)

2. Right compound:
   - Five-membered ring with two methoxy groups (O–CH3)

### f)
1. Left compound:
   - Five-membered ring with methoxy group (CH3), hydroxyl (OH), and methylene group (CH2)

2. Right compound:
   - Five-membered ring with methoxy group (
Transcribed Image Text:Determine the structural relationship between the compounds in each of the pairs that follow. They may be unrelated, identical (the same compound), constitutional isomers, diastereomers, or enantiomers. - Identify the optically active (chiral) compounds and any _meso_ compounds. - Assign a configuration (R or S) to all stereocenters. - Name all compounds so that the name reflects the structure unambiguously. ### a) 1. Left compound: - Structure: CHO, NH2, HO, CH2OH - Groups: Aldehyde, amine, hydroxyl, and primary alcohol groups 2. Right compound: - Structure: CH2OH, OH, H, NH2, CHO - Groups: Primary alcohol, hydroxyl, hydrogen, amine, and aldehyde groups. ### b) 1. Left compound: - Cyclohexane with wedge and dash substituents: H (wedge) and CH3 (dash) 2. Right compound: - Cyclohexane with wedge and dash substituents: CH3 (wedge) and H (dash) ### c) 1. Left compound: - Central carbon with four groups: H, CH3, Cl, Ph (phenyl) - Stereochemistry indicated by solid wedges (towards viewer) and dashed lines (away from viewer) 2. Right compound: - Central carbon similar to left, arranged differently: Ph, CH3, Cl, H - Stereochemistry indicated by solid wedges (towards viewer) and dashed lines (away from viewer) ### d) 1. Left compound: - Cyclic structure with Cl (wedge) and H (dash), carbonyl (C=O) present. 2. Right compound: - Cyclic structure with H (wedge) and Cl (dash), carbonyl (C=O) present. ### e) 1. Left compound: - Six-membered ring, carbonyl group, methyl branch (CH3) 2. Right compound: - Five-membered ring with two methoxy groups (O–CH3) ### f) 1. Left compound: - Five-membered ring with methoxy group (CH3), hydroxyl (OH), and methylene group (CH2) 2. Right compound: - Five-membered ring with methoxy group (
Expert Solution
Step 1: Interpretation of given problem

Given are organic compounds.

Isomers are compounds that have same molecular formula but different structural formula. 

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