Back to marketplace

Qualitative Test for Hydrocarbons

No description yet. This curated deck is ready for daily study.

Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

Hydrocarbons – can be grouped into four structural classes

Back (Answer)

Alkane Alkene Alkyne Aromatic hydrocarbon

#2
Front (Question)

test to distinguish different hydrocarbons:

Back (Answer)

Bayer’s Test Br2 Test (light and dark) Tollen’s Test Sulfuric acid test

#3
Front (Question)

the experiment includes the generation of this

Back (Answer)

ethyne

#4
Front (Question)

used to determine the presence of ethyne

Back (Answer)

flammability test

#5
Front (Question)

oxidizes alkenes to geminal diols

Back (Answer)

dilute aqueous potassium permanganate

#6
Front (Question)

means two -OH groups

Back (Answer)

diol

#7
Front (Question)

OH groups on adjacent carbons

Back (Answer)

geminal

#8
Front (Question)

oxidized to geminal diketones

Back (Answer)

alkynes

#9
Front (Question)

in this reaction, the potassium permanganate is reduced to this of manganese dioxide

Back (Answer)

brown precipitate

#10
Front (Question)

what the potassium permanganate is reduced to

Back (Answer)

manganese dioxide

#11
Front (Question)

which solution is the potassium permanganate soluble in

Back (Answer)

water

#12
Front (Question)

neither water nor potassium permanganate is soluble in this

Back (Answer)

hydrocarbon

#13
Front (Question)

where the water and hydrocarbon reaction takes place and is somewhat slow

Back (Answer)

water-hydrocarbon interface

#14
Front (Question)

except cycloalkanes react with bromine

Back (Answer)

unsaturated hydrocarbons

#15
Front (Question)

these are the only hydrocarbons that is negative in br2 (dark)

Back (Answer)

alkane

#16
Front (Question)

hydrocarbons positive in Br2 (light)

Back (Answer)

all hydrocarbons

#17
Front (Question)

usually used as solvents because they are unreactive toward both bromine and hydrocarbons that have multiple bonds

Back (Answer)

cyclohexane/carbon tetrachloride/tetrachloromethane

#18
Front (Question)

undergo an addition reaction with bromine

Back (Answer)

alkenes and alkynes

#19
Front (Question)

its bond becomes a single bond and one bromine atom becomes bonded to each of the carbons that had shared the double bond

Back (Answer)

alkene

#20
Front (Question)

its bond undergoes addition becoming a single bond but the carbons that had been joined by the number of its bond will now hold two bromine atoms

Back (Answer)

alkyne

#21
Front (Question)

react with concentrated sulfuric acid at room temperature to produce alkyl sulfonic acid

Back (Answer)

alkenes

#22
Front (Question)

highly polar and is soluble in the polar sulfuric acid with sufficient stirring

Back (Answer)

alkyl sulfonic acid

#23
Front (Question)

not soluble in the polar concentrated sulfuric acid concentrated sulfuric acid, but dissolves as it reacts and the mixture is stirred

Back (Answer)

alkene

#24
Front (Question)

not capable of forming hydrogen bonds, while the sulfuric acid and the alkyl sulfonic can

Back (Answer)

alkene