close presentation Organic reaction maps drag and drop

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close presentation Organic reaction maps drag and drop Task 1 reaction types Task 1

close presentation Organic reaction maps drag and drop Task 1 reaction types Task 1 answers Task 2 matching structures to names Task 2 answers Task 3 reagents and conditions Task 3 answers

close presentation Task 1. Drag a colour block to label arrows as oxidations, reductions

close presentation Task 1. Drag a colour block to label arrows as oxidations, reductions substitutions and additions or eliminations (some arrows may be more than one type of reaction) propanenitrile propylamine propan-1 -ol propanamide propanal propane propan-2 -ol propanoic acid chloropropane ethylpropanoate propanone Substitution Elimination propanoyl chloride propene Addition Reduction Oxidation propanoic acid anhydride answers

close presentation Task 1. Answers propylamine Reduction Addition propanenitrile Addition Substitution propan-1 -ol Addition

close presentation Task 1. Answers propylamine Reduction Addition propanenitrile Addition Substitution propan-1 -ol Addition Oxidation propanamide Substitution propanal Substitution propane Oxidation propan-2 -ol propanoic acid Addition Reduction Substitution Reduction Oxidation Elimination chloropropane Substitution ethylpropanoate propanone Addition Substitution Elimination propene Addition Oxidation propanoyl chloride Reduction Substitution propanoic acid anhydride Task 1

close presentation Task 2. Drag the structures alongside the correct names propanenitrile propylamine propanamide

close presentation Task 2. Drag the structures alongside the correct names propanenitrile propylamine propanamide propan-1 -ol propanal propanoic acid propane propan-2 -ol ethyl propanoate chloropropane propanoyl chloride propene propanoic acid anhydride answers

close presentation Task 2. Answers propanenitrile propylamine propanamide propan-1 -ol propanal propanoic acid propane

close presentation Task 2. Answers propanenitrile propylamine propanamide propan-1 -ol propanal propanoic acid propane propan-2 -ol ethyl propanoate chloropropane propanoyl chloride propene propanoic acid anhydride Task 2

close presentation Task 3. Drag and drop the correct reagents and conditions onto the

close presentation Task 3. Drag and drop the correct reagents and conditions onto the correct arrows in the next slide

NH 3 H 2 Nickel catalyst H 2 O / Na. OH 1. Li.

NH 3 H 2 Nickel catalyst H 2 O / Na. OH 1. Li. Al. H 4 (ether) 2. H 2 O K 2 Cr 2 O 7 / H 2 SO 4 distil off product propylamine close presentation H 2 O / HCl cold propanenitrile SOCl 2 H 2 O / HCl heat K 2 Cr 2 O 7 / H 2 SO 4 reflux ethanol propan-1 -ol propanamide propanal Ethanol / H 2 SO 4 reflux propane propan-2 -ol propanoic acid chloropropane H 2 O ethylpropanoate propanone propanoyl chloride propene H 2 Nickel catalyst Ethanol / H 2 SO 4 reflux K 2 Cr 2 O 7 / H 2 SO 4 reflux H 2 O / H 2 SO 4 heat H 2 O / H 2 SO 4 HCl 1. Li. Al. H 4 (ether) 2. H 2 O propanoic acid anhydride KOH in ethanol Al 2 O 3 heat answers

close presentation Task 3. Answers H 2 Nickel catalyst propylamine NH 3 propan-1 -ol

close presentation Task 3. Answers H 2 Nickel catalyst propylamine NH 3 propan-1 -ol H 2 O / HCl cold K 2 Cr 2 O 7 / H 2 SO 4 distil off product propanal H 2 O / Na. OH propane propan-2 -ol propanenitrile propanamide K 2 Cr 2 O 7 / H 2 SO 4 reflux 1. Li. Al. H 4 (ether) 2. H 2 O propanoic acid Ethanol / H 2 SO 4 reflux K 2 Cr 2 O 7 / H 2 SO 4 reflux chloropropane SOCl 2 Al 2 O 3 heat H 2 Nickel catalyst H 2 O / H 2 SO 4 heat ethyl propanoate KOH in ethanol H 2 O / HCl heat H 2 O propanone NH 3 ethanol HCl propanoyl chloride propene 1. Li. Al. H 4 (ether) 2. H 2 O / H 2 SO 4 Ethanol / H 2 SO 4 reflux propanoic acid anhydride Task 3