I’m new to organic chemistry
Start by reviewing atoms, bonds, molecular geometry, and structure drawings.
Start with: Organic Chemistry, Chapter 1: Why This Chapter?
RedLectern topic
Core ideas for representing carbon compounds, explaining their structures and reactions, and interpreting basic evidence about molecular structure.
For: Learners beginning organic chemistry, returning to it, or seeking a focused route into a core topic.
After this page you can: Represent simple organic molecules, identify common functional groups and stereochemical features, explain basic reaction steps, and use introductory spectra to support a structural proposal.
Page reviewed
Organic chemistry is the study of carbon compounds. Carbon atoms can form four covalent bonds and bond to one another in chains and rings, creating a wide variety of molecular structures.
It is studied by representing molecules, relating their structures to functional groups, and tracing how bonds change in reactions. Learners can practice drawing structures, considering stereochemistry, and using spectroscopy to gather evidence about molecular structure.
Start by reviewing atoms, bonds, molecular geometry, and structure drawings.
Start with: Organic Chemistry, Chapter 1: Why This Chapter?
Use the course outline to review structures, transformations, mechanisms, and stereochemical reasoning.
Start with: Organic Chemistry I
Begin with IR patterns, then compare what other common structure-determination techniques examine.
Start with: Interpreting Infrared Spectra
Carbon’s bonding and molecular geometry help explain the range of structures studied in organic chemistry.
The course introduces principles for understanding organic molecular structure and reactivity.
Covalent bond
A bond formed when an electron pair is shared between atoms.
Functional group
A group of atoms within a molecule that has characteristic chemical behavior.
Sketch a carbon atom with four single bonds, then draw a second carbon joined to it by one of those bonds.
Each carbon can have four covalent bonds; the two-carbon structure can be represented with a single bond between the carbon atoms.
Stereochemistry considers how three-dimensional arrangement distinguishes molecules, including mirror-image forms.
The course objectives include using stereochemical considerations when analyzing mechanisms and transformations.
Chiral
A molecule is chiral if it is not identical to its mirror image.
Chirality center
A common chirality center is a tetrahedral carbon bonded to four different groups.
Does a tetrahedral carbon bonded to H, OH, CH3, and CH2CH3 have four different groups attached?
Yes. Those four groups differ, which is the common structural cause of chirality described for a tetrahedral carbon.
A reaction mechanism describes the stages of a chemical transformation, including the bonds broken and formed.
This section gives rules and examples for using curved arrows to represent electron movement in polar mechanisms.
Reaction mechanism
A detailed description of what happens at each stage of a chemical transformation.
Homolytic cleavage
Bond cleavage in which one electron remains with each product fragment.
In a homolytic bond cleavage, how many electrons from the broken bond go to each fragment?
One electron goes to each product fragment.
Functional groups classify molecules by characteristic chemical behavior and help organize reaction patterns.
The course includes substitution and elimination reactions, carbonyl chemistry, and aromatic compounds.
Alkene
An organic compound containing a carbon–carbon double bond.
Which functional group is present in a molecule with a C=C bond?
The C=C bond is the carbon–carbon double-bond functional group found in alkenes.
Mass spectrometry, IR, and NMR are techniques of structure determination for organic molecules.
This section summarizes what mass spectrometry, IR, NMR, and UV spectroscopy examine.
Infrared spectroscopy
A technique that can provide structural information from characteristic functional-group absorption bands.
An IR spectrum has a strong, broad O–H absorption. Which kind of functional group could this support?
It could support the presence of an alcohol O–H group; an O–H absorption is listed among characteristic IR bands.
No recent updates are available.
Jonathan Clayden, Nick Greeves, and Stuart Warren · 2012
The second edition presents an explanatory approach aimed at helping readers understand the subject.
Michael B. Smith and Jerry March · 2007
The publisher describes it as a resource for planning and executing synthetic reactions.
Francis A. Carey and Richard J. Sundberg · 2007
Springer describes coverage of structural topics and basic mechanistic types, including stereochemistry and carbonyl chemistry.
Francis A. Carey and Richard J. Sundberg · 2007
Springer describes the volume pair as a foundation for advanced undergraduates or beginning graduate students to understand and use organic chemistry research literature.
Listed as Organic Chemistry courses: