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Part-2 organic chem

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

Card preview (24)

#1
Front (Question)

carbon sp3

Back (Answer)

tetrahedral 109.5 4 singles

#2
Front (Question)

carbon sp2

Back (Answer)

trigonal planar 120 1 double and 2 single

#3
Front (Question)

carbon sp

Back (Answer)

linear 180 1 triple and 1 single bond or 2 double bond

#4
Front (Question)

oxygen sp3

Back (Answer)

tetrahedral - electron bent - molecular

#5
Front (Question)

oxygen sp2

Back (Answer)

trigonal planar - electron linear- molecular

#6
Front (Question)

nitrogen sp3

Back (Answer)

tetrahedral- electron pyrimidal- molecular

#7
Front (Question)

nitrogen sp2

Back (Answer)

trigonal planar- electron bent- molecular

#8
Front (Question)

nitrogen sp

Back (Answer)

linear- electron linear - molecular

#9
Front (Question)

more symmetrical, less polar will? bp

Back (Answer)

lowering boiling point

#10
Front (Question)

melting point

Back (Answer)

may or may not follow this general rule, as a more symmetrical molecule typically packs better, requiring more energy (higher melting point) to melt the solid

#11
Front (Question)

bond length

Back (Answer)

length character the shorter the bond,

#12
Front (Question)

alkane formula

Back (Answer)

C(n)H(2n+2)

#13
Front (Question)

bp in hydrocarbons vs. electronegative

Back (Answer)

hydrocarbons, bp increase with more number of carbon (molecular weight or molar mass) electronegative atoms, increase bp when compared to a molecule of similar weight with a less polar group or if hydrogen bonding is possible

#14
Front (Question)

organic compounds tend to be

Back (Answer)

combustible

#15
Front (Question)

base acid nucleophile electrophile

Back (Answer)

base- proton acceptor acid- proton donor nucleophile- electron donor with the formation of a bond lewis base electrophile- electron acceptor lewis acid

#16
Front (Question)

strong acids because

Back (Answer)

cb is 1) charge 2) size, electronegativity 3) resonance 4) inductive

#17
Front (Question)

iso propopylnol isopropylcyclopentane

Back (Answer)

three carbons coming off of the carbons

#18
Front (Question)

isobutane

Back (Answer)

ch3 off of the second carbon Ch3(ch3) coming off of chch3 total carbon 4 even with the coming off one

#19
Front (Question)

isopentane

Back (Answer)

ch3 (ch3)coming off of the chch2ch3 total carbon 5 even with the coming off one

#20
Front (Question)

neopentane

Back (Answer)

ch3( ch3)2 coming off from both sides of cch3 total carbon 5 even with the coming off ones

#21
Front (Question)

alkane alkene alkyne

Back (Answer)

alkane= c-c alkeyne= c=c alkyne= c (triple bond) c

#22
Front (Question)

nitrile

Back (Answer)

R-c (triple bond) n

#23
Front (Question)

alcohol

Back (Answer)

R-OH

#24
Front (Question)

amines 1st degree 2nd degree 3rd degree

Back (Answer)

R-NH2 R-NH-R R-N-R n with three r coming off of it l R