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D. Chirality 6. Build two models of 2-butanol, a chiral molecule. Are the mirror images of your two models superimposable on each other? If they are, change something so they are not. If you have done this correctly, you will be able to set up the two models as non-superimposable mirror images of each other. You now have the two enantiomers of 2-butanol. Draw the mirror images of 2- butanol below. Note this molecule has a carbon atom, a "stereocenter", attached to four different groups. What are these four different groups? Is 2-butanol a primary, secondary or tertiary alcohol? To determine this, consider the carbon directly attached to the -OH group, how many carbons are directly bonded to it? We will look at the difference between primary, secondary and tertiary alcohols at the beginning of lab. Primary, secondary and tertiary alcohols display very different reactivity in chemical reactions. Look up and describe below a possible reason for this.

D. Chirality 6. Build two models of 2-butanol, a chiral molecule. Are the mirror images of your two models superimposable on each other? If they are, change something so they are not. If you have done this correctly, you will be able to set up the two models as non-superimposable mirror images of each other. You now have the two enantiomers of 2-butanol. Draw the mirror images of 2- butanol below. Note this molecule has a carbon atom, a "stereocenter", attached to four different groups. What are these four different groups? Is 2-butanol a primary, secondary or tertiary alcohol? To determine this, consider the carbon directly attached to the -OH group, how many carbons are directly bonded to it? We will look at the difference between primary, secondary and tertiary alcohols at the beginning of lab. Primary, secondary and tertiary alcohols display very different reactivity in chemical reactions. Look up and describe below a possible reason for this.

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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D. Chirality 6. Build two models of 2-butanol, a chiral molecule. Are the mirror images of your two models superimposable on each other? If they are, change something so they are not. If you have done this correctly, you will be able to set up the two models as non-superimposable mirror images of each other. You now have the two enantiomers of 2-butanol. Draw the mirror images of 2- butanol below. Note this molecule has a carbon atom, a "stereocenter", attached to four different groups. What are these four different groups? Is 2-butanol a primary, secondary or tertiary alcohol? To determine this, consider the carbon directly attached to the -OH group, how many carbons are directly bonded to it? We will look at the difference between primary, secondary and tertiary alcohols at the beginning of lab. Primary, secondary and tertiary alcohols display very different reactivity in chemical reactions. Look up and describe below a possible reason for this.
Transcribed Image Text:D. Chirality 6. Build two models of 2-butanol, a chiral molecule. Are the mirror images of your two models superimposable on each other? If they are, change something so they are not. If you have done this correctly, you will be able to set up the two models as non-superimposable mirror images of each other. You now have the two enantiomers of 2-butanol. Draw the mirror images of 2- butanol below. Note this molecule has a carbon atom, a "stereocenter", attached to four different groups. What are these four different groups? Is 2-butanol a primary, secondary or tertiary alcohol? To determine this, consider the carbon directly attached to the -OH group, how many carbons are directly bonded to it? We will look at the difference between primary, secondary and tertiary alcohols at the beginning of lab. Primary, secondary and tertiary alcohols display very different reactivity in chemical reactions. Look up and describe below a possible reason for this.
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