
Alkynes
Chemistry
University
NGSS covered
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9 questions
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1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the correct IUPAC name for the following structure
(Z) 1-cyclopentyl-3,6-dimethylhept-3-en-1-yne
(E) 1-cyclopentyl-3,6-dimethylhept-1-yn-3-ene
(Z) 1-cyclopentyl-4,7-dimethylhept-4-en-2-yne
(E) 1-cyclopentyl-3,6-dimethylhept-3-en-1-yne
Tags
NGSS.HS-PS1-3
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the correct IUPAC name for the following compound?
4-(1-bromopropyl)-1-hexen-5-yne
4-allyl-5-bromo-1-hexyne
3-(1-bromopropyl)-5-hexen-1-yne
5-bromo-4-ethynyl-1-heptene
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which of the following improperly describes the physical properties of an alkyne?
relatively nonpolar
nearly insoluble in water
less dense than water
insoluble in most organic solvents
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which of the following alkynes has the lowest boiling point?
1-pentyne
2-hexyne
3-pentyne
1-butyne
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
In trans-hept-4-en-2-yne the shortest carbon-carbon bond is between carbons
2 and 3
1 and 2
3 and 4
4 and 5
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Among the compounds water, but-1-yne, but-2-yne, and ethane, which are stronger acids than ammonia?
but-1-yne and ethane
water and but-1-yne
water and ethane
but-1-yne and but-2-yne
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Why is a terminal alkyne favored when sodium amide (NaNH2) is used in an elimination reaction with 2,3-dichlorohexane?
The strong base deprotonates the terminal alkyne and removes it from the equilibrium
The resonance favors the formation of the terminal rather than internal alkyne
The positions of the Cl atoms induce the net formation of the terminal alkyne
The terminal alkyne is not favored in this reaction
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