1.5 Flashcards

(33 cards)

1
Q

carbonyl group

A

carbon double bonded to an O, functional group responsible for properties in aldeydes and ketones

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2
Q

methanal

A

formaldehyde

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3
Q

aldehydes

A

terminal carbonyl group

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4
Q

ketones

A

non-terminal cabonyl group

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5
Q

properties of ketones and aldehydes

A

polar due to c-o bonds (D-D), stonger than alkanes but weaker than alchohols, lower boilng point and less soluble than alcohols, good solvents due to ability to dissolve polar and non-polar which depends on how big R group is, small aldehydes/ketones = completely soluble, size ++ = solubility down

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6
Q

reactions of carbonyl groups

A

controlled oxidation and hydrgoenation

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7
Q

controlled oxidation

A
primary alcohols = aldehyde + water
secondary = ketone + water
tertirary = no reaction
alcohol  =(O) aldehyde/ ketone + water
(o) = oxidzing agent = oxygen rich compounds = cr2o72- and KMnO4
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8
Q

hydrogenation

A

need high temp, preassure + catalyst

aldehyde/ ketone + h2 = alcohol

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9
Q

carboxylic acid

A

weak acid with a carbonyl and alcohol group attaches, sour/ tangy taste, polar, strong h-bonding and dipole-dipole, small Ca are soluble in water but solubility decreases as size does, higher melting, bigger np end = more ld, neutralizes

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10
Q

ester

A

organic compound cotnaining a carbonyl group bonded to a O bonded to a R group, responsible for odour and flavourings, no hydroxyl group = less polar than ca = no H-bonding, small ester are more soluble in water due to polarity of c-o bonds. less soluble than Ca + lower boiling, polarity = similar to aldehyde/ketones, organic salt

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11
Q

ester reactions

A

esterfication, hydrolysis and saponification

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12
Q

ca reactions

A

contorlled oxidization of a aldhyde

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13
Q

esterfication

A

ca + alcohol with h2so4 makes ester + water

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14
Q

hydrolysis

A

ester + strong base = alcohol + salt of acid

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15
Q

nh

A

amino functional group

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16
Q

adrenline

17
Q

amine

A

oraginc compound relates to ammonia which has an N boned to an alkyl group, polar, strong unpleasant odour as fishy, offensive decay and decomp odour, n-h bonds allow h-bonidng, higher boiling than similar sized hydrocarbons, smaller = more soluble, weak bases that neturalize, found in plants and have medicinal properties

18
Q

degree of amines

A

primary has the most h-bonding where as 3 has none

19
Q

amide

A

ca + amine, caontains a cabronyl group bonded to a N, weak base, insoluble in water, small = slightly soluble, acetaminophen, urea

20
Q

main component in pain killers

A

acetaminophen

21
Q

found in urine of mamals and used as a fertlizer

22
Q

amine reaction

A

preperation - alkyl halide + ammonia/1 or 2 amine = amien + h___

23
Q

amide reactions

A

condensation reaction - ca + amine = amide + water

hydrolysis - amide + water = ca + amine

24
Q

3 types of linkages

A

c-c (playstic), c-o (ester) and c-n (Amine)

25
polymer
large molecule made up of repeating monomer sequences
26
types of polyemers
homopolymers (only one type of monomer, can only do add reactions) and copolymers (two types, add and condestaion reactions)
27
addition polymer reactions
free radical (Initiation), chain porpgation (propogates) and termination via terminator
28
condensation polymer reaction
a difunctional group is added to make either polyesters or polyamides following reaction and can keep going but will stop when a singular is added to the compound
29
natural polymers
silk, cotton, wool, linen, cellulose
30
synthetic polymers
plastic, nylon, ryon, polyester
31
polymerization
the process of chain reactions by which monomers are linked together to form a polymer
32
cross linkage
polymers which are unstaurated are attracted to one another via intemroleculer attraction between polymers and there form interlocking bond like a net between polymers making the structure strong, rigid and inflexible
33
properties of polymers
unreactive - unsaturated alkanes mouldable / flexible - weak intermolecular foces, np strength - degree of cross linkage diff side groups make diff properties