Symmetry The World of Organic Molecules. What is Symmetry?

Slides:



Advertisements
Similar presentations
C.I. 3.6 Optical Isomerism.
Advertisements

Chemistry 2100 Lecture 8. Enantiomers Enantiomers: Enantiomers: Nonsuperposable mirror images. –As an example of a molecule that exists as a pair of.
Chapter 7. Stereochemistry.
Unit 3 – Stereochemistry
Organic Chemistry Stereochemistry. Isomers compounds with the same molecular formula but not identical structures.
Bio Organic Chemistry Stereochemistry. Review of Isomers.
Chapter 6 Stereochemistry
Topics in Stereochemistry. Chiral Carbon Atoms A sp 3 hydbridized carbon atom with four different substituents is chiral. Chiral carbon atoms are also.
Stereoisomerism Nanoplasmonic Research Group Organic Chemistry Chapter 5.
Stereochemistry.
Isomers Larry J Scheffler Lincoln High School IB Chemistry
4 Types of Isomers Structural Isomers/(Constitutional)
1 Stereoisomers Review: –Structural Isomers: Compounds that have the same molecular formula, but differ in the structural arrangement of atoms. Examples:
3 3-1 Organic Chemistry William H. Brown & Christopher S. Foote.
© 2003 Thomson Learning, Inc. All rights reserved General, Organic, and Biochemistry, 7e Bettelheim, Brown, and March.
Chapter 5 Stereochemistry The Arrangement of Atoms in Space; The Stereochemistry of Addition Reactions.
Stereochemistry The arrangement of atoms in space By: Dr. Manal F. Abou Taleb Organic Chemistry, 5 th Edition L. G. Wade, Jr. chapter 5.
Stereochemistry & Chiral Molecules. Isomerism Isomers are different compounds with the same molecular formula 1) Constitutional isomers: their atoms are.
CHE 311 Organic Chemistry I Dr. Jerome K. Williams, Ph.D. Saint Leo University.
Chirality “Handedness”: Right-hand glove does not fit the left hand. An object is chiral if its mirror image is different from the original object. Chapter.
Chemistry 106 You need: Text & Lab Book (+ all lab safety stuff) Online Notes access:
Chirality Chirality - the Handedness of Molecules.
Isomers Isomers: different compounds with the same molecular formula Constitutional isomers: isomers with a different connectivity Stereoisomers: isomers.
Chapter 7 Stereochemistry. 7.1 Molecular Chirality: Enantiomers.
Stereochemistry 1. Stereoisomerism 2. Chirality
Types of Isomers.
We have already covered two kinds of isomerism: Constitutional Isomers (structural isomers) Stereoisomers.
Introduction to Organic Chemistry 2 ed William H. Brown
Lecture Nine : Stereochemistry
Chemistry 2100 Chapter 15. Enantiomers Enantiomers: Enantiomers: Nonsuperposable mirror images. –As an example of a molecule that exists as a pair of.
Chapter 7 - Stereochemistry Enantiomers of bromochlorofluoromethane Non-superimposable mirror images – Enantiomers.
PHARMACEUTICAL ORGANIC CHEMISTRY LEC 2. QI: Arrange the following sets in order of decreasing priority -H, -C 2 H 5, -CH 3, -C(CH 3 ) 3, -CH(CH 3 ) 2.
Symmetry The World of Organic Molecules. What is Symmetry?
Stereochemistry. Required background: Shapes of molecular structures Isomers, conformers Essential for: 1. Understanding of S N 1, S N 2, E1, E2, and.
Stereochemistry 240 Chem Chapter 5 1. Isomerism Isomers are different compounds that have the same molecular formula.
Organic Chemistry, 8th Edition L. G. Wade, Jr.
Isomers Are different compounds with the same molecular formula
14.5 Chiral Molecules An object whose mirror image is identical to the original and can be superimposed on it is achiral. Objects such as hands that have.
Structural, Geometric, Enantiomer
Stereochemistry of organic compounds
Chirality A molecule is chiral if its two mirror image forms are not superimposable upon one another. A molecule is achiral if its two mirror image forms.
Organic Chemistry Lesson 5.
Chemical isomers.
The 3-D Shape of Molecules
CHE2060 Lecture 6: Chirality
Chirality “chiral” Greek for hands chiral =
Isomers Molecules with same molecular formula but their respective atoms are arranged differently in space 1.
SAM GIRLSCOLLEGE, BHOPAL
P. 289.
University of California,
Stereoisomerism and Chirality Unit 5.
The World of Organic Molecules
Only three of a maximum possible four stereoisomers exists for the molecule shown. These include a pair of enantiomers and a single meso compound. Meso.
Chapter 5: Stereochemistry
Stereoisomerism and Chirality Unit 5.
Stereoisomerism.
Chirality “chiral” Greek for hands chiral =
Kinds of Isomers © Prentice Hall 2001 Chapter 4.
Chirality All three-dimensional objects are either symmetric or asymmetric. A symmetric molecule can be superimposed on its mirror image. An asymmetric.
Chirality “chiral” Greek for hands chiral =
Chapter 6 Principles of Stereochemistry ***Bring Your Model Kits to Class!***
Chapter 7 STEREOCHEMISTRY
handedness in Molecules
Stereoisomerism and Chirality Unit 6.
240 Chem Stereochemistry Chapter 5.
Organic Chemistry Lesson 3.
Chapter 12 Organic Compounds with Oxygen and Sulfur
240 Chem Stereochemistry Chapter 5.
1.Structural 2.Stereo isomers - geometric - optical
240 Chem Stereochemistry Chapter 5.
Presentation transcript:

Symmetry The World of Organic Molecules

What is Symmetry?

Symmetry is likeness of shape or arrangement about a center.

Does this Design Have Symmetry?

Symmetry About a Plane Anything that contains an internal mirror plane is symmetric. Anything that lacks an internal mirror plane is asymmetric.

Chirality Asymmetric objects have an interesting property called Chirality which means “handedness”. Chiral objects can have two different forms, a right-handed and left-handed form which are mirror images of each other but are not exactly alike.

Examples of Chiral Objects Your Hands and Feet Gloves and Shoes Golf Clubs Computer keyboard

Are the Following Objects Chiral or Achiral? Baseball Bat RefrigeratorCarBicycle Your Face ForkNailScrew

Chiral Molecules? A carbon atom with four different groups bonded to it creates a stereocenter in the molecule. Most molecules which contain one or more stereocenters lack an internal plane of symmetry and are therefore chiral.

Enantiomers The right-handed and left-handed forms of a chiral molecule make up a pair of stereoisomers called enantiomers. Enantiomers are not identical, but they have the same physical properties such as melting point boiling point, etc. So why do we care about this subtle form of stereoisomerism?

Chirality in the Biological World When chiral organic compounds interact with living systems, the two enantiomers often interact very differently. This is because living systems are chiral at many different levels in many ways: - our hands and feet are chiral (of course) - our taste buds are chiral - our olfactory sensors are chiral - our enzymes are chiral - our enzymes are chiral

Carvone

Limonene

Aspartame

Ibuprofen

Summary Molecules which lack symmetry are Chiral Chiral molecules have right-handed and left- handed forms Right-handed and left-handed molecules interact with living systems in very different ways. –Different smell –Different taste –Different drug effects