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
Aromatics
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
Alkyl halides
Hydrocarbon with halogen attached F, Cl, Br, I Follow alkane rules and add position number with prefix chloro, Fluoro, bromo or iodo
26
Ethers
``` 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
Cyclical alkanes alkanes or alkynes
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
Aldehyde
Carbonyl functional group on end carbon | Follow hydrocarbon rules and use suffix "al"
29
Ketones
Carbonyl group in middle of chain Follow hydrocarbon rules and use suffix "one" Add position number infront of suffix Ex. 3-methylpentan-2-one