Polymers and Life Flashcards

1
Q

What is a phenol group

A

A benzene ring with an -OH attached

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2
Q

Carbonate reaction with carboxylic acids

A

Acid-base reaction in which the CO2- is the base. H+ is the acid and carbon dioxide is formed

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3
Q

Phenol and alcohol reaction with carbonate

A

Do not have a large enough concentration of H+ ions to make carbon dioxide so the reaction will not fizz

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4
Q

Reaction which breaks down an ester

A

Hydrolysis, the two types are acid and alkali

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5
Q

Naming esters

A

The ending -oate comes from the parent acid which is attached to the carbon in the ester linkage, the ending -yl comes from the other substance used which is attached to the oxygen in the ester linkage

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6
Q

Amine function groups and properties

A
  • NH2 group

- Lone pair of electrons on the nitrogen allows amines to act as bases

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7
Q

Amides functional group

A
  • CONH-

- Formed by reacting an amine with either a carboxylic acid or a acyl chloride

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8
Q

Acid hydrolysis

A

The ester linkage breaks down and the NH2 group becomes NH3+

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9
Q

Alkaline hydrolysis

A

The ester linkage breaks down and the COOH group becomes COO-

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10
Q

Zwitterions

A

A molecule which contains both negatively and positively charge groups. They are often used in buffer solutions

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11
Q

Chiral centres and optical isomers

A

A chiral centre is a carbon atom with four different groups bonded to it.

Optical isomers are molecules with the same chemical structure, but they are mirror images of themselves around the chiral centre.

This means they are non-superimposable

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12
Q

Enantiomers

A

The different optical isomers are called enantiomers

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13
Q

The three levels of protein structure

A

Primary - the order of the amino acids

Secondary - the coiling of the primary structure to form a helix or a pleated sheet

Tertiary - the folding of the secondary structure

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14
Q

Bonds in the tertiary structure

A

Instantaneous dipole-induced dipole bonds between non-polar side chains

Hydrogen bonds between between the peptide links

Ionic bonds between ionisable side chains

Covalent bonds between when -SH groups oxidise to -S-S- groups

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15
Q

What are enzymes

A

High specific catalysts which are sensitive to pH and temperature and are subject to competitive inhibition

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16
Q

What are inhibitors

A

Molecules which fit into the active site of an enzyme but cannot be catalysed

17
Q

What is a pharmacophore

A

The part of a molecule which gives it a pharmaceutical abilities

18
Q

What is a nucleotide

A

A sugar, phosphate, and a base bonded together

19
Q

What are the four bases and which bonds with which

A

Cytosine bonds with Guanine via three hydrogen bonds

Adenine bonds with Thymine via two hydrogen bonds

20
Q

Transcription

A
  • A section of the DNA unzips
  • RNA nucleotides join together and create a complimentary strand to the unzipped DNA
  • The mRNA strand leaves the DNA
  • The DNA zips back up
21
Q

Translation

A
  • mRNA from transcription enters the ribosomes
  • tRNA joins to the RNA via the anti-codon
  • The tRNA joins different amino acids together creating a protein chain