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Structural Isomer
Atoms are arranged differently with same molecular formula
Geometric Isomer
Same order of connectivity, but different arrangement
Optical Isomer
Non superimposable mirror images with a chiral carbon center
Conditions for optical isomer
chiral carbon center
Four different atoms/groups bonded to same carbon
Substitution for Alkene and addition Alkane (Br2 reagent)
Added to an alkane with presence of UV light and a slow substitution will occur, it slowly decolorise from orange/brown very slowly
added to an alkene, it will rapidly decolorise as an unsaturated molecule undergoing addition
Addition (Halogenation) reagent: X2/HX
Where a halogen molecule or hydrogen halide adds across a double bond
Hydrogenation ( Alkene to Alkane) Reagent: Ni at 150, or Pt
Where a hydrogen molecule adds across the double bond of an alkene to form an alkene
Hydration ( Alkene to Alcohol) Reagent: H20/H+ H2SO4- dilute
When alkene reacts with water in acidic conditions to form an alcohol
L3 Reactions
Lucas Reagent: Conc Hcl/ZnCl2
removal of an alcohol group and replace with haloalkane
Tertiary Alcohol: immediate reaction
Secondary Alcohol: slow reaction around 2 min
Primary Alcohol: very slow, no visible reaction
Alcohol Oxidation
Reagent: SOCl2,PCl3,PCl5
Primary: alcohol to aldehyde to carboxylic acid
Secondary: alcohol to ketone
Distillation (aldehyde) reagent: H+/Cr2O72-
Aldehydes have a lower boiling point than alcohol, so the reaction mixture is heated and forms evaporation and a condenser is set up to remove aldehyde
Reflux ( Carboxylic Acid) H+/MnO4- or H+/Cr207-
Reaction mixture is heated to increase the rate of reaction and a condenser is set up to condense the aldehyde back into reaction mixture increasing the yield forming a carboxylic acid
Distillation (Aldehyde) P.A.D
Purpose: to seperate substance based on different boiling point, preventing futher reactions
Advantages: can be used to purify mixtures, by separating the substance
Disadvantage: only allows separation based on boiling point
Reflux ( Carboxylic Acid) P.A.D
Purpose: allows heating of reaction mixtures to max yield and reaction rates without the loss of volatile substance
Advantage: max yield while increasing the rate of reaction
Disadvantage: superheating and risk breakage of glassware
Yield
Amount of product obtained from a chemical reaction, eg: higher yield more product
Volatile
Tendency of a substance to vaporise into a gas at a given time