Transtitions Flashcards
Moving from primary halide to primary amine
+ NH3
Ammonia will replace halide group, resulting in protonated amine
- H+
Deprotonates amine, resulting in primary amine
Moving from primary halide to alcohol
+ NaOH
OH replaces halide leaving NaX(halide)
Moving from alcohol to ether
+Na or K
Replaces the H group on OH
+Alkyl halide
Alkyl group replaces Na/K
Moving from alcohol to carboxylic acid
\+ KMnO4 Primary Alcohol becomes carbobylic Purple -> brown Or \+ K2Cr2O7 Alcohol becomes carbonyl then carboxylic (only if carbonyl is aldehyde) Orange -> green
Moving from carboxylic to amide
+SOCl2
Cl replaces OH, leaving SO2 + HCL
+ amine (RNH2)
Replaces Cl group, losing H
Moving from amide to carboxylic
+ H+, H2O
Or
+ NaOH, H2O (Produces anion)
Requires heat, seperates amide into amine
Moving from carboxylic to ester
\+ROH, H+ Replaces H on OH, produces water Or \+SOCl Cl replaces OH, leaving SO2 + HCL \+ ROH Replaces Cl
Moving from aldehyde to carboxylic
\+Tollens reagent Algehyde is oxidized, gaining O Tollens becomes silver metal Or \+ K2Cr2O7 green to orange
Moving from alkene to alkylhalide
+ HX (Halide)
Forms alkylhalide
Moving from alkene to alcohol
+H2O, H+
Forms alcohol
Moving from alkyne to alkane
+2H2
Hydrogenation
Moving from alkene to diol
+KMnO4, 0 degrees
Forms diol with double bond oxidation
Moving from diol to carboxylic
+KMnO4
(Primary and secondary alcohol)
Forms carboxylic, oxidation
Moving from diol to ketone
+KMnO4
(primary and tertiary alcohol)
Forms ketone, oxidation
ampere
1 coulomb per second