Organic reactions. Reagents and conditions

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H2C=CH2 + H2 ->reagents and conditions
H2 with Ni (catalyst) and temperature
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H2C=CH2 + H20 ->
H2O (steam) 330C 6MPA H3P04 or H2SO4
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H2C=CH2 + HBr
concentrated HBr room temperature
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H2C=CH2 + H2O + (O) ->
Cold dilute acidified KMnO4
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H2C=CH2 + (O) -> ,,,
Hot concentrated H2SO4
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KMnO4 changes
pink to colourless
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H3C-CH2-Br + H2O -> H3C-CH2-OH + HBr
NaOH or H2O and heat under reflux
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H3C-CH2-Br +KCN -> CH3-CH2-CN + KBr
KCN in aqueous solution of ethanol and heat under reflux
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H3C-CH2-Br +NH3 -> CH3-CH2-NH2
NH3 in aqueous ethanol and heat under pressure
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H3C-CH2-Br + NaOH -> CH2=CH-CH3 + H2O + NaBr
NaOH in ethanol
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H3C-CH2-OH +HCl -> H3C-CH2-Cl + H2O
HCl in situ and heat under reflux
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H3C-CH2-OH + SOCl2 -> H3C-CH2-Cl + ....?
HCl +SO2
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H3C-CH2-OH + PCl5 -> H3C-CH2-Cl + ...? +r and c?
POCl3+ HCl r is PCl5 and room temperature
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3H3C-CH2-OH + PI3 ->3 H3C-CH2-I +...? r and c?
H3P04 r is PI3 in situ and temperature
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esterification? (has equilibrium)
Heat under reflux and concentrated H2SO4
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H3C-CH2-OH -> H2C=CH2 + H20
A2O3 hot powder / SiO2 / pumice/ H2SO4
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oxidation of alcohols
Acidified K2Cr2O7 and dilute H2SO4 and reflux
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r-CN -> R-COOH
dilute H2SO4 and heat
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R-CHO +NaCN -> r-CH(OH)-CN
NaCN in situ and dilute H2SO4
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R-CN -> R-CH2-NH2
Na and ethanol
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Carbonyl group + 2,4= DTPH + colour ppt?
2,4-dinitrophenylhydrazine deep orange
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Aldehyde + Tollen's reagent
AgNO3 (mild oxidation) in excess NH3 solution and MIRROR EFFECT
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Aldehyde + Fehling's solution
warmed and clear blue to opaque red/orange
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Other cards in this set

Card 2

Front

H2C=CH2 + H20 ->

Back

H2O (steam) 330C 6MPA H3P04 or H2SO4

Card 3

Front

H2C=CH2 + HBr

Back

Preview of the front of card 3

Card 4

Front

H2C=CH2 + H2O + (O) ->

Back

Preview of the front of card 4

Card 5

Front

H2C=CH2 + (O) -> ,,,

Back

Preview of the front of card 5
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