Exam 4- Organic And Nuclear Flashcards

1
Q

What is the current definition of organic chemistry?

A

the chemistry of carbon interacting with all other atoms on the periodic table

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2
Q

what are organic compounds?

A

Carbon containing molecules

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3
Q

Alkanes

Gemetric shape, hybridization, trend, bonding, suffix

A

tetrahedral in shape because all Cs have 4 coordination
sp3 hybridized
Cn H2n+2
There are all C or H all single bonded
(longest chain prefix)-ane

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4
Q

What is the skeletal structural formula?

A

Each line represents two carbons, one at each end.
Also called bond line structure

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5
Q

What is an Isomer, what are the two types and their differences?

A

When two or more molecules have the same chemical formula but different structures.
Structural Isomer vs Geometric Isomer
Ex C4H10 is Butane and Methyl Propane. same name but different structures
Ex Cis 2 Butane and Trans 2 Butane are geometric isomers

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6
Q

Cis vs Trans given the structure

A
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7
Q

Alkyl Group

A

ending in -yl
substituted groups of carbon atoms on the largest continuous chain
“side chain”

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8
Q

What is the most reactive cycloalkane and why?
What are the most stable?

A

cyclopropane because we are changing the bond angle, forcing e- together to ~60 degrees
pent- and hex- because of the ideal bond angle 109.5

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9
Q

Describe Chair vs Boat structures and which is more stable. Why

A

In the boat form two hydrogens are in the axial position and are too close together, making it unstable.
In the chair form, the two hydrogens are further from each other, making this the more stable form for cyclohexane

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10
Q

Cis vs Trans
which has a higher melting point

A

Substituted groups on the same side of the carbon chain are cis
Substituted groups on different sides of the carbon chain are trans
Trans Isomers have higher mp due to the ability to “stack” or pack close together.
Because of this, trans are considered more stable

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11
Q

Three types of intermolecular forces and their order of strength

A

Hydrogen> Dipole-Dipole > London Dispersion

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12
Q

Hydrogen bonding

A

A bond where H is attached to an F, O, or N. It is a type of Dipole Dipole

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13
Q

Dipole Dipole force

A

two polar molecules bonding positive to negative

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14
Q

London Dispersion force

A

also known as van der waals
Localized dispersion of electron cloud in a bond over one atom for a brief moment in time-temporary dipoles

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15
Q

Intermolecular forces impact the _________ of the various organic compounds and ______________

A

Intermolecular forces impact the physical properties of the various organic compounds and certain chemical properties

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16
Q

Physical properties of Alkanes

A

non polar
Stable and unreactive unless energy is put into the system
does not dissolve in water
as you increase the chain length you will increase the melting and boiling points

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17
Q

Alkenes

A

General form Cn H2n
sp2 hybridized, coordination number is 3 so trigonal planar
MUST HAVE AT LEAST 1 DOUBLE BOND
Suffix becomes -ene
Two double bonds suffix is -diene
-Must use a number to denote location of the double bond

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18
Q

Naming Alkenes

A

no such things as a single carbon (no meth) since it needs a double bond
ends in -ene, indicate cis or trans
The double bond sets the number direction, lowest number wins

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19
Q

What suffix means all single bonds?
What suffix means double bonds are present?

A

-ane
alkanes

-ene
Alkenes

20
Q

What suffix means “side chain” (as opposed to not on the parent chain)

A

-yl
alkyls

21
Q

Carboxylic acid

A

R-COOH, where a c-o is double bonded
Suffix -oic
Start numbers with the carbonyl carbon
highest melting point due to all intermolecular forces
Great lewis acid

22
Q

Amine

A

R-NH2
suffix -amine
Start numbering with the NH2 C
Lewis BASE
lewis bases, more carbons=more basic

23
Q

Amide

A

R-CONH2, where C and O are double bonded
suffix- amide
higher BP than the amine because of the carbonyl-has all 3 intermolecular forces
Also basic but less so than amine due to carbonyl

24
Q

Ester

A

R-COO-R, where a C- are double bonded
suffix -oate
Name the last R first, then (carbon # prefix)-oate

25
Q

What are functional groups

A

a group of atoms that determines many of a molecule’s properties.

26
Q

Alkynes

A

contains a triple bond
suffix -yne
no cis or trans, must indicate which carbon has the triple bond

27
Q

Aromatic ring

A

a cyclene with alternating double bonds
ex: benzene

28
Q

Ether

A

R-O-R
An oxygen attached to two R groups (R can be methyl, ethyl….)
Ethers are polar because of the central O
ends in -oxy
very volatile , lower melting point, may be a better lewis base

29
Q

Alcohol

A

R-OH
carbon chain must have OH, gets lowest number possible
suffix -ol
Lewis aicd

30
Q

Ketone

A

R-CO-R
where O is double bonded
“carbonyl group”
Suffix -one
usually the CO double is near the middle of the chain (not at the end)
fruity smells

31
Q

Aldehyde

A

R-CHO
Where C to O is double bonded
suffix -al
always number aldehydes first
do not hydrogen bond so lower melting point.
Aledehydes make up “earthy smells”
lewis acid

32
Q

What is a substituent?

A

A group other than −H bonded to the carbons of an organic molecule.

33
Q

Thiols

A

R-SH
lower melting point
very volatile, only has london dispersion forces-non polar

34
Q

Coordination number

A

number of atoms and unshared pairs of electrons on the atom of interest.
Directly related to its hybridization

35
Q

Which functional group has the highest melting point?

A

carboxylic acids, or those with hydrogen bonding

36
Q

What is high vapor pressure and which functional group is a good example of this?

A

Ether- turns to gas easily, lowest melting point

37
Q

What is the best lewis acid functional group

A

Carboxylic acids

38
Q

The longer the chain the ________the acid

A

the longer the chain the weaker the acid

39
Q

What can determine high melting points?

A

the ability to hydrogen bond

40
Q

Beta Decay

A

A neutron is converted into a proton, and an electron gets ejected.
Bad bad bad to have a free charged electron floating through space to hit into anything
Atomic number goes up 1

41
Q

Alpha Decay

A

Production of a helium atom, referred to as an alpha particle, spits out 2 protons and 2 neutrons and has NO CHARGE. Not dangerous.
Protons go down 2 but atomic goes down 4

42
Q

Positron Decay/Emission

A

Positron emission happens when a proton is converted into a neutron. What is ejected is a positively charged electron, a positron.
Atomic number goes down 1

43
Q

Electron Capture

A

like reverse beta decay. Sucking an electron from the cloud into the nucleus. Releases gamma rays. E is on left, not right. Atomic number will go down 1

44
Q

Highest effectiveness factor

A

Beta. Most dangerous form of radiation because it is charged and can hit a person and be absorbed, changing the cells it hits.
Alpha can be absorbed easily
Gamma can pass straight through, unless it cant then its dangerous.

45
Q

Dehydration Synthesis/Esterification

A

Combination of two molecules with the elimination of a water molecule
Ex: one compound donating an H and another compound donating an OH. Together they break off and make H2O

46
Q

Weak Force vs Strong Force

A

Weak- interaction that occurs between subatomic particles
Strong- Force taht acts over short distances but is very strong, attracts + to +, overcomes coulomb forces