Table of contents

1. A Review of General Chemistry5h 5m
2. Molecular Representations1h 14m
3. Acids and Bases2h 46m
4. Alkanes and Cycloalkanes4h 17m
5. Chirality3h 39m
6. Thermodynamics and Kinetics1h 22m
7. Substitution Reactions1h 48m
8. Elimination Reactions2h 30m
9. Alkenes and Alkynes2h 9m
10. Addition Reactions3h 19m
11. Radical Reactions1h 58m
12. Alcohols, Ethers, Epoxides and Thiols2h 42m
13. Alcohols and Carbonyl Compounds2h 17m
14. Synthetic Techniques1h 26m
15. Analytical Techniques:IR, NMR, Mass Spect7h 3m
16. Conjugated Systems6h 13m
17. Ultraviolet Spectroscopy51m
18. Aromaticity2h 34m
19. Reactions of Aromatics: EAS and Beyond5h 1m
20. Phenols55m
21. Aldehydes and Ketones: Nucleophilic Addition4h 56m
22. Carboxylic Acid Derivatives: NAS2h 51m
23. The Chemistry of Thioesters, Phophate Ester and Phosphate Anhydrides1h 10m
24. Enolate Chemistry: Reactions at the Alpha-Carbon1h 53m
25. Condensation Chemistry2h 9m
26. Amines1h 43m
27. Heterocycles2h 0m
28. Carbohydrates5h 53m
29. Amino Acids4h 20m
30. Peptides and Proteins2h 42m
31. Catalysis in Organic Reactions1h 30m
32. Lipids 2h 50m
33. The Organic Chemistry of Metabolic Pathways2h 52m
34. Nucleic Acids1h 32m
35. Transition Metals6h 14m
36. Synthetic Polymers1h 49m

5. Chirality

Chirality

Organic Chemistry

5. Chirality

Chirality

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Problem 46c

Textbook Question

Classify the following objects and molecules as chiral or achiral.
(c) <IMAGE>

Verified step by step guidance

Step 1: Understand the concept of chirality. A molecule is chiral if it cannot be superimposed on its mirror image, often due to the presence of an asymmetric carbon atom (a carbon bonded to four different groups). Achiral molecules, on the other hand, can be superimposed on their mirror images and often have a plane of symmetry.

Step 2: Examine the structure of the molecule provided in the image. Look for any carbon atoms that are bonded to four distinct groups. If such a carbon exists, the molecule is likely chiral.

Step 3: Check for symmetry in the molecule. If the molecule has a plane of symmetry or a center of symmetry, it is achiral. Use visual inspection or draw the mirror image of the molecule to determine if it can be superimposed.

Step 4: Consider any stereocenters (chiral centers) in the molecule. A stereocenter is typically a carbon atom with four different substituents. If the molecule has one or more stereocenters, it is likely chiral unless symmetry cancels out the chirality.

Step 5: Based on the analysis of the molecule's structure, symmetry, and stereocenters, classify the molecule as chiral or achiral. Ensure that you carefully evaluate all relevant features before making the classification.

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Chirality

Chirality refers to the geometric property of a molecule that makes it non-superimposable on its mirror image. A chiral molecule typically has at least one carbon atom bonded to four different substituents, resulting in two distinct enantiomers. This property is crucial in organic chemistry as it affects the behavior of molecules in biological systems and their interactions with polarized light.

Achirality

Achirality describes molecules that are superimposable on their mirror images, meaning they do not have a chiral center. These molecules can often be symmetrical, and their structures do not lead to distinct enantiomers. Understanding achirality is important for distinguishing between chiral and achiral substances in various chemical contexts.

Stereoisomerism

Stereoisomerism is a form of isomerism where molecules have the same molecular formula and connectivity but differ in the spatial arrangement of atoms. This includes both enantiomers (chiral) and diastereomers (not necessarily chiral). Recognizing stereoisomers is essential for classifying molecules as chiral or achiral, as the arrangement of substituents can significantly influence their properties and reactivity.

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Related Practice

Textbook Question

Classify the following objects and molecules as chiral or achiral.

(k)

Textbook Question

As we learned in Chapter 2, we don't need to show hydrogens bonded to carbons when drawing organic molecules using line-angle formulas. At asymmetric centers, however, we often show the hydrogen. Why? When might it be unnecessary to show the hydrogen at a chiral center?

Textbook Question

Identify the following molecules as chiral or achiral. If chiral, draw the nonsuperimposable mirror image and verify its nonsuperimposability.

(e)

Textbook Question

Classify the following objects and molecules as chiral or achiral.

(a) <IMAGE>

Textbook Question

Determine whether the following objects are chiral or achiral.

Textbook Question

The chiral BINAP ligand shown in Figure 8-8 contains no asymmetric carbon atoms. Explain how this ligand is chiral.

Textbook Question

Draw three-dimensional representations of the following compounds. Which have asymmetric carbon atoms? Which have no asymmetric carbons but are chiral anyway? Use your models for parts (a) through (d) and any others that seem unclear.c. ClHC═C═C(CH3)21-chloro-3-methylbuta-1,2-diened. ClHC═CH―CH═CH21-chlorobuta-1,3-diene