Organic Chemistry
Vocabulary:
i.) Oxidation in organic molecules involves: (select all that apply)
a.Gain of bonds to H
b.Gain of bonds to C
c.Gain of bonds to EN atoms
d.Loss of bonds to H
e.Loss of bonds to C
f.Loss of bonds to EN atoms
g.Gain of electrons
h.Loss of electrons
j.none of these
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ii.) Ring strain is made up of ____ and _______ strains.
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iii.)
In 1H NMR the __ tells the functional group present.
a.chemical shift
b.coupling
c. integration
In 1H NMR the __ tells how many neighbors are present within 3 bonds.
a. chemical shift
b. coupling
c. integration
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iv.)
Diastereomers ____ have the same bonds.
a. always
b. sometimes
c. never
Diastereomers ____ have the same chemical and physical properties.
a. always
b. only in a chiral environment, or with plane polarized light
c. never
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v. Rank the following by the amount of ring strain:
cyclohexane, cyclobutane, cyclopropane, cyclopentane
The most ring strain is: ______________
Then: ______________ has a lot of ring strain.
______________has minimal ring strain.
And______________has nearly no ring strain.
Ring strain is made up of angle strain. Less the inner angle in the cyclic compound more will be the strain. Cyclic compound with carbon number more than seven will also experince ring strain.
Organic Chemistry Vocabulary: i.) Oxidation in organic molecules involves: (select all that apply) a.Gain of bonds...
Organic Chemistry: Vocabulary: I.) Pi bonds are the ____ bond between two atoms. a. 1st b. 2nd only c. 3rd only d. 1st or 2nd e. 2nd or 3rd f. 1st, 2nd, or 3rd Pi bonds hold electrons ___ two atoms. a. directly between b. above and below c. in front and behind d. directly between OR above and below e. above and below OR in front and behind f. any of these Pi bonds can be made with overlap...
Organic Chemistry: Vocabulary I.) In general elimination reactions will form the _ stable alkene. a. more b. less This is typically the alkene with: a. more substituents b. less substituents. c. cannot tell The exception is when we have an __ mechanism with a _. a. E1, hindered poor nucleophile b. E1, unhindered poor nucleophile c. E2, hindered strongly basic nucleophile d. E2, unhindered strongly basic nucleophile ________________________________________________________________________________________________ II.) Staggered rotamers have a _________ degree torsional angle. Nucleophiles are ___...
Organic Chemistry Coupling in NMR: Question 1: What equation is used to determine the number of sub-peaks seen in a single H NMR signal? (type in answer) ______________________________________________ Question 2: When a single H NMR peak is split into 3 pieces it's a ____. (type in answer) ______________________________________________ Question 3: When a single H NMR peak has no coupling it's called a __. (type in answer) _____________________________________________ Question 4: OH and NH hydrogens ___ show coupling in free-rotating systems. a.)...