Unit 2: Organic Chemistry Flashcards

0
Q

Trigonal planar

A

Carbon with two single bonds and one double

120

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1
Q

Carbon with 4 single bonds

A

Tetrahedral 109.5

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2
Q

Bent 109

A

Oxygen with two lone pairs and two bonding

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3
Q

Carbon with two double or one triple

A

Linear
Increased melting point due to easy packing
180

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4
Q

Nitrogen with 3 bonding pairs and one lone pair

A

Trigonal pyramidal

120

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5
Q

Hydroxyl

A
OH 
Polar .... Hydrogen bond 
Make one HB 
Follow hydrocarbon rules and use suffix "ol" 
Ex. Propan-2-ol
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6
Q

Alkoxy

A

Oxygen bonded between two carbons
Polar with dd
Accepts 1 HB

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7
Q

Amine

A

Nitrogen bonded to carbons or hydrogens with 1 lone pair
Primary: HB and makes 2
Secondary: makes 1 HB
Tertiary: dd accept on HB

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8
Q

Double bonded o

A

Carbonyl group
Polar and dd
Accept one HB from h2o

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9
Q

-COOH

A

Carboxyl
1 HB 1dd
Make 1 HB and accept 1
Follow hydrocarbon rules and use suffix “oic acid”

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10
Q

Esters

A
C double bonded o and single bonded o
2 dd
Accepts 2 from h2o
Identify the chain with c=o as parent 
Add alkyl group infront of main chain and leave space 
Ex. Methyl propanoate
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11
Q

Amide

A
-CON
1+2 HB 3: two dd
1: makes 2 accept 1 HB
2: accept 1 make 1 HB
3: accept 2 HB 
Name the c=o as parent and use suffix "amide" 
Name other alkyl groups attached 
Use N as position number for any alkyl group attached to nitrogen 
Ex. N-methylethanamide
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12
Q

Make vs. accepting hydrogen bond

A

Make: N,F,O bonded to H
Accept: N,F,O not bonded to H

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13
Q

Large molecules

A

Higher melting point due to stronger mp

Less polar overall so less soluble

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14
Q

Addition reaction

A

A double or triple bond is broken and atoms are attached to the organic
If both reactants are asymmetrical then two isomers are made

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15
Q

Elimination reaction

A

Atoms are removed from a molecule to form a double or triple bond
If organic is asymmetrical then two isomers are made

16
Q

Substitution reactions

A

A hydrogen or functional group is replaced with a different group
Esters don’t do substitution reactions

17
Q

Oxidation reactions

A

Forms more carbon to oxygen bonds less to carbon to hydrogen bonds
An oxidizing agent [O] must be added
C-O to C=O
H to OH

18
Q

Reduction reactions

A

Forms less carbon to oxygen bonds and more carbon to hydrogen bonds
Must add a reducing agent [H]
Substitute any OH with H
then change C=O to C-O

19
Q

Condensation reactions

A

Two organic molecules join releasing water

20
Q

Hydrolysis reactions

A

Water splits an organic molecule into two smaller organics

C-O and C-N bonds can only be broken

21
Q

Polymers

A

Very large molecules made up of small repeating monomers

Occur in nature or can be manufactured to fulfill a particular purpose

22
Q

Addition polymers

A

Monomers with double bonds are joined together

Ex. Ethene + ethene = polyethene

23
Q

Condensation polymers

A

Monomers are joined together by ester or amide bonds

24
Q

Aromatics

A

Benzene(6 carbon ring) rings
Hydrocarbons with resonance structures containing rings (more stable) with 1.5 bonds
Benzene is usually your man chain and used as root Ex. 1-ethyl-4-propylbenzene
If benzene is attached to a chain with 7 or more carbons the benzene is considered a side chain called phenyl Ex. 3-methyl-5-phenyloctane
Strong LD due to easy packing higher MP
D.I.D

25
Q

Alkyl halides

A

Hydrocarbon with halogen attached
F, Cl, Br, I
Follow alkane rules and add position number with prefix chloro, Fluoro, bromo or iodo

26
Q

Ethers

A
Alkoxy functional group ROR'
Name longest chain as parent 
Name short chain Alkoxy group with prefix "oxy" 
Ex. 1-methoxy ethane 
Polar DD
Accepts HB
27
Q

Cyclical alkanes alkanes or alkynes

A

Hydrocarbons with ring structure
Follow appropriate rules
Ring is always main chain and add “cyclo” infront of root name
If double or triple bond present must be between carbon 1 and carbon 2
3-methylcyclobut-1-ene

28
Q

Aldehyde

A

Carbonyl functional group on end carbon

Follow hydrocarbon rules and use suffix “al”

29
Q

Ketones

A

Carbonyl group in middle of chain
Follow hydrocarbon rules and use suffix “one”
Add position number infront of suffix
Ex. 3-methylpentan-2-one