Kluger Organic Lab Final

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Can you name the Organic Lab Final?

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Reactant that limits the amount that can be formed
Water loving and charge polarized
Polyamides that have less than 50 amide links
To purify solids
Reaction of bifunctional molecules with the elimination of a small molecule
Used when liquids aren't mutually soluble and the desired material distills at a temperature below 100
Substance that loses electron
Transferring a solute from one solvent to another
Removes water from liquids
The expected amount of product
Used to prevent toxic gases from escaping by neutralizing it
Formed when the monomer units add to one another
Enzymes with large polymeric amino acid molecules
Food and Drug Administration
Metal ions that bind the protein to the substrate
Substance that reduces swelling
Liquid mixture with a constant boiling point
Used to carry out a chemical reaction at constant temperature
Aldehyde or ketone derivative used as a detection reagent in thin layer chromatography
Electron donating group attached to aromatic ring
Causes organic layer to be less soluble in water
Tests for methyl ketones and acetaldehydes
Water fearing and nonpolar
Evidence of purity for solids
Groups with unshared pairs of electrons that are activators
compound with a positive and negative charge on adjacent atoms
In its natural position
Reactant used to polymerize styrene
Reaction of 2 free radicals to make a covalent bond and end the polymer
Difunctional molecule containing a basic nitrogen group and acidic carboxylic acid group
Used to put product on the obtain IR
Formation of a bathtub ring by soaps reacting with hard water
Substance that provides a chemical means of communication
Isomeric forms for the same structure that exist because of an alpha hydrogen transfer
Cluster of ball with dirt and grease particles
Physical property of the substance under the conditions of analysis
Polymer formed by polymerizing the same monomer
Liquid condensed from vapor during distillation
Substance that gains electrons
Separates miscible liquids by differences in boiling points
Electron pair donor
Any of a large class of synthetic organic dyes that contain -N=-N-
Breaks down to produce NO2 or NO
Non-protein part of enzymes that bind to the protein substrate
Most electronegative element that wants to gain electron
Electron pair acceptor
Fat or lard with three different fatty acids
Carboxylic acid salt
Ion with a positively charged carbon atom
Tests for unsaturation and forms trans 1,2 dibromo products
Capable of decaying through the action of living organisms
Tests for carboxylic acid salts
Atoms, molecules, or ions with unpaired electrons
Quantity of a product found to be formed in a chemical reaction
To separate crystalline product from the 'mother liquors' which contains impurities
Free radical addition to another styrene monomer
Reaction of a fat or oil with aqueous hydroxide
Hemolytic cleavage of O-O bond of benzoyl peroxide
Polymers formed by polymerizing two different monomers
Reference book that classifies dyes and pigments by chemical structure
Hydrogens on the carbon right next to the carbonyl carbon
Used to detect components of a compound by the Rf values
non-halogen groups with atoms that are more electronegative than carbon
Electron withdrawing group attached to aromatic ring
Biological coenzyme used to carry out an organic reaction under milder condition
Substance that relieves pain
Atom that is displaced as stable species taking with it the bonding electrons
Liquid produced after filtering a suspension of a solid in a liquid
Mean of expressing the accuracy of a test
Substance that reduces fever
Makes use of acidic properties of gases
Aldehyde or ketone derivative used to detect the carbonyl functionality of a ketone
Practical aspect of telling how successful the synthesis of the product my the amount produced
Food, drugs, and cosmetics dyes
Stationary phase used in this layer chromatography
Developing phase
Removes excess acid
Combine 2 identical molecules
Less electronegative element that wants to lose electrons
Carbanions that are formed by the reaction of base with alpha hydrogens
Phase that doesn't move and has low affinity
tests for unsaturation and forms 1,2 diol products
Used for compounds with high boiling point
Volatile constituent of seeds, barks, roots of plants
B-hydroxycarbonyl compound formed when an enolate ion adds to an electron deficient compounds

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