Organic Chem Flashcards

(37 cards)

1
Q

Describe Alkanes

A

-Hydrocarbon with only single bonds between carbon atoms
-General formula: CnH2n+2
-Homologous series because they differ by the number of repeating units
-Saturated because single bonds, carbon has 4 bonds, it’s filled.

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2
Q

What is an organic compound?

A

A chemical compound which contains carbon.

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3
Q

What are the exceptions to organic compounds (contain carbon but are not organic)?

A

Carbides - SIC
Carbonates - CO3
Cyanides - CN-
Simples oxides of carbon - CO2

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4
Q

For the alkane family, what is the effect of molecule size on boiling point?

A

The larger the size of the compound has on average, has a higher boiling point.

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5
Q

What is a akyl branch?

A

Consists of only carbon and hydrogen atoms.

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6
Q

Describe Cycloalkanes

A

-Cyclic hydrocarbons have a closed ring structure
-When naming prefix cyclo in front of the parent chain name
-General formula: CnHn

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7
Q

Describe Alkenes

A

Hydrocarbons that contain double bonds (carbon-carbon).
Alkenes are MORE reactive then Alkanes.
General Formula: CnH2n
-Unsaturated because of double bonds.

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8
Q

Describe Allynes

A

-Hydrocarbons that have carbon-carbon triples bonds.
-Alkynes are EVEN MORE reactive then either Alkanes or Alkenes
-General formula: CnH2n-2
-Unsaturated because of triple bonds.

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9
Q

What is an important rule when naming Alkenes and Alkynes?

A

-The chain is numbered from the end closed to the multiple bond.

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10
Q

What is the general formula for Cycloalkenes?

A

CnH2n-2

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11
Q

What is the general formula for Cycloalkynes?

A

CnH2n-4

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12
Q

What are aromatics?

A

-Benzene (C6H6) is called aromatics because the molecules have alternating double bonds.
-Very Stable
-Used for building blocks for molecules in body such as hormones.
-Benzene can also be called resonance
-Aromatics are not saturated or saturated but they behave like saturated molecules
-Anything that’s not aromatic is called aliphatic

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13
Q

How do you name a benzene ring when it’s a branch?

A

-Phenyl group.

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14
Q

What are structural isomers?

A

-Molecules that have the same general formula but different structural formulas (different arrangement of atoms, imagine the model kits from class.)
-Same chemical formula, different structural model.

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15
Q

How do double bonds (saturation) affect boiling point?

A

-Leads to lower boiling points because of decreased intermolecular forces compared to saturated compounds.

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16
Q

How do branches affect boiling point?

A

-Leads to Lower boiling points because of reduced surface area for intermolecular interactions.

17
Q

How is crude oil separated in a furnace?

A

-Crude oil separated on the basis of boiling point is called fractional distillation
-Small molecules have low boiling points and rise to the top of the tower
-Larger molecules have higher boiling points so they condense near the bottom.

18
Q

What is cracking?

A

-Refineries used the process of cracking to break large hydrocarbons into smaller ones.
-If there’s a decade (10 carbon) just count the carbons in each section. (10-3=7)
C-C-C-C-C-C-C-C-C-C
C-C-C + C-C-C-C-C-C-C

19
Q

Describe Halides

A

-Organic halides are organic compounds in which one or more hydrogen atoms have been replaced by halogen atoms. (Group 17 ions; F, CL, Br, I).
-This halogen is considered a functional group (An atom or group which gives the molecule its specific properties-> types of reactions a molecule can undergo.)

20
Q

What are the prefixes for the Halide functional groups?

A

F - Fluoro
Cl - Chloro
Br- Bromo
I - Iodo

21
Q

Describe alcohols

A

-An alcohol is an organic compound containing the hydroxyl (OH) functional group.
-As a result of hydroxyl alcohols form hydrogen bonds.
-A hydrogen bond occurs when a hydrogen atom that is bonded to strong electronegative atom (like O2) is attracted to a lone pair of electrons in an adjacent molecule.
-These strong intermolecular forces means alcohols have a higher boiling point than other hydrocarbons of similar molar mass.
-Polar and dissolve in water

22
Q

How to name polyalcohol?

A

-Contains more than one hydroxyl group
-The “e” is not dropped in the name, just like dienes and diynes.

23
Q

Conditions for addition reactions of organic compounds?

A

-Need double or triple bonds.
The unsaturated hydrocarbons (multiple bonds, Alkenes or Alkynes) react with small diatomic molecules like halogens (F2), hydrogen, or hydrogen halides (HF)
-Needs heat or catalyst
It breaks the multiple bond which gives it space to attach
-Unsaturated->saturated

24
Q

Conditions for substitution reactions of organic compounds

A

-A hydrogen in an alkane or benzene ring (not saturated but acts as if it is) is replaced with another atom or group of atoms.
-Reactant needs to be saturated
-Saturated -> Saturated (single bonds)

25
Describe elimination reaction in organic compounds
-Saturated -> Unsaturated (single to double bonds) -Only single to double bonds, no triple -Involves removing atoms or group of atoms from adjacent carbon atoms in an organic compound. (Opposite of addition).
26
Describe complete combustion reaction of organic compounds
-A hydrocarbon (fuel) reacts with oxygen (g) to produce carbon dioxide (g) and water Vapor (H20g) -Happens when there is excess oxygen present. (More than enough.) -If not told otherwise assume combustion is complete
27
Describe incomplete combustion reaction of organic compounds
-A hydrocarbon fuel reacts with oxygen (g) to produce carbon monoxide (COg) solid carbon (C) (g), along with carbon dioxide and water Vapor. -Will happen if there’s insufficient oxygen. -C (s) is in the form of soot.
28
Describe Carboxylic acids
-Organic compounds that contain carboxyl (COOH) (O attached to the carbon has a double bond) functional group. -Always at the end of a chain or as a branch. -Have low Ph. -Name them by replacing the “Ane” ending of the alkanes name with “oic acid” (Ane -> Anoic)
29
Describe a condensation reaction
-Where a carboxylic acid reacts with another reactant to form an organic compound and H2O
30
Describe Esterification reactions
-Esterification is a specific type of condensation reaction where a carboxyl acid reacts with an alcohol to produce an ester and water.
31
What is an ester?
-The ester functional group (COO) is similar to carboxyl group but the H attached to the O is gone and a C is there. -The ester is made from part of the carboxyl acid and part of the alcohol. -Their formation is always: Carboxyl acid + alcohol -> ester +water
32
What are polymers?
-Polymers are large chain molecules made by joining many smaller molecules called monomers -Natural polymers include protiens, carbohydrates, and lipids. -Synthetic polymers include plastics, nylon and more -Polymers are ether addition or condensation reactions. -Polymers are strong because of all covalent bonds.
33
What are polymers?
-Polymers are large chain molecules made by joining many smaller molecules called monomers -Natural polymers include protiens, carbohydrates, and lipids. -Synthetic polymers include plastics, nylon and more -Polymers are ether addition or condensation reactions. -Polymers are strong because of all covalent bonds.
34
How to name an ester?
2 parts: 1. The name of the alkyl group (group of hydrogen and carbons.) from the alcohol. 2. The acid name with the ending “oate.”
35
When should a compound end in “ol”
-When there is an OH attached but it’s not carboxyl (COOH)
36
How does the bromine test work (for saturation)?
-If bromine is added (orange color) to solution and there’s no reaction it’s saturated (single bonds). The color remains. -If bromine is added and it loses its orange color, the solution is unsaturated (multiple bonds). (It’s an addition reaction).
37
When should you end the compound with “oate”
-When you have a double bond of oxygen and a single oxygen. (Not a carboxyl (COOH) or hydroxyl (OH)).