Chapter 4 Summary

About this set

Created by:

msimmons33  on January 17, 2011

Subjects:

honors organic chemistry

Description:

summary from book

Log in to favorite or report as inappropriate.
Pop out
No Messages

You must log in to discuss this set.

Chapter 4 Summary

cycloalkane
saturated cyclic hydrocarbon with the general formula CnH2n
1/16
Preview our new flashcards mode!

Study:

Cards

Speller

Learn

Test

Scatter

Games:

Scatter

Space Race

Tools:

Export

Copy

Combine

Embed

Order by

Terms

Definitions

cycloalkane saturated cyclic hydrocarbon with the general formula CnH2n
free rotation is _____________ in cycloalkanes greaty reduced
cis-trans isomers exist in disubstituted cycloalkanes
cis isomer both substituents on the same face
trans isomer substituents on opposite faces
stereoisomers isomers that have the same connections between atoms but different 3D arrangements
three kinds of strain that contribute to the overall energy of a cycloalkane angle strain, torsional strain, and steric strain
angle strain the resistance of a bond angle to compression or expansion from the normal 109.5
torsional strain the energy cost of having neighboring C-H bonds eclipsed rather than staggered
steric strain the repulsive interaction that arises when two groups attempt to occupy the same space
cyclohexane strain-free because it adopts the "chair" configuration
chair conformation all bond angles are near 109 and all neighboring C-H bonds are staggered
axial position oriented up and down
equatorial position on the sides
Ring-flip interconverts axial and equatorial positions
susbtituents on the ring are more stable in the ________ because ______ equatiorial position because axial substituents cause 1, 3 - diaxial interactions

First Time Here?

Welcome to Quizlet, a fun, free place to study. Try these flashcards, find others to study, or make your own.

Set Champions

Scatter Champion

42.3 secs by ehop21