1/13
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai |
|---|
No analytics yet
Send a link to your students to track their progress
Reduction with sodium in Liquid ammonia
Starts with triiple bond
Uses Na, NH3, and H2O
Ends with double bond no different substituents seen in product
Hydrohalogenation of Alkynes
Starts with triple bond
Uses HBr (excess) or X, or includes bezne to add extra bond
Ends with Two Br or X on the same carbon same side single bonded (cis)
Double halogenation of an alkyne
Starts with triple bond
Uses Cl2 or X2, LiCl or LiX, and AcOH
Uses Br (excess) or X, with CCl4 when has hook not a straight line
Ends with double bond with Cl or X on two carbons beside each other on different side (trans)
Hydroboration -Oxidation
Starts with triple bond
Uses BH3, THF, H2O2, NaOH, H2O
Oxygen with double bonds gets added where triple bond ends
Meruric Ion
Strats with triple bond
Uses H2SO4, HgSO4, and H2O
ENds with an oxygen pn the secnd carbon of the product (total four)
Alkylation of a terminal alkyne (connected to hydrogens)
Startes with triple bonds
Uses NaH, CH3I, Et2O
Ends with a methyl gorups at the end of the truiple bond
Double Dehydrohalogenation
Startes with single two Br or X on different carbonc (trans) beside each other
Uses NaNH2 excess
Ends with no Br or X and wiht a triple bond
Alkylation with carbonyl compounds
Startes with tripple bond
Uses EtMgBr: CH3CHO, H, H2O
Ends iwth a OH and methyl at the end of the triple bond
Hydrogenation with Lindlar’s catalyst
Starts wth triple bond with CH3 at the end
Uses H2, and Lindalr’s catlayst
ends with a double bond and Both substituents facing the sam eway (cis)
Hydrogenation with Pt, PD-C, and Ra-Ni
Startes with triple bond
uses H2, PD-C, and Et2O
End with single bond and CH3 attahced ot the end of it ( triple bond)
Radical addtition with Anti-Marlovlv
Startes with triple bond
Uses HBr or X, with ROOR
Ends with a double bond and Br or X attached to it
Heck reaction
Ring is open (hexane)
Uses Pd(OAc)2, Ph3P, and heat
Ends with the ring closed (pentane) with leaving gorup gone
Suzuki
Ring is open
Uses Pd(Ph3P)4, Ph3P, NaHCO3, and H2O
Ends with ring close and no substients
Hydration / haloghydrin
Starts with triple bond
Use Br2 or X2, with H2O
Ends with both OH and Br or X on opposite sides on diffrent carons with Oxygen with a double bond