halogenation of a-carbons Target Product CH3 нс, 0 Hgc Br Br CH3 O CH3 H3C click...
synthesis of cyclic acetals Target Product H₂C H2C CH3 click on a reagent to add it to the synthesis p (0.202 sec) Link Reload Reactants Reload Reagents Reload Pathway / Workspace Products Reactants CH3 0- нс о CH3 НО- он Н.С re.edugen.wiley.com/cgibin/tutorial/Reaction Tutorial Reactants он Н.С. -Сн, нс- нс 0 Н.С Сн. HS - HEC CH3 HS Reagents OH OS-OH O (catalyst) OH H₂O OSOH ! o (cold, dilute) H2 (excess) Pt or Pd or Ni Pathway (0.000 sec)
malonic ester synthesis Target Product G. Click on a reactant to add it to the synthes (0.204 sec) Link Reload Reactants Reload Reagents Reload Pathway / Workspace Products Reactants Br. Br. CI Reactants witCH San C! CH, Reagents 1. Mix Reactants in DMSO or THF (solvent) (2. H2O (Aqueous workup)) OH O=S-OH H2O II O (hot, dilute) -O Na+ CH3
Use the provided reactants and reagents to generate the target product Reactants Reagents Target P HaC HBr ROOR, Light H,c CH CH H,C Br2 CCI4, light CH3 2 step(s) may generate muitiple praducts 3 stepfs) may generale muliple stereoisomers Select 읕 reagent fron the reagent fran@ CH CH (0.463 sec) Link Reload Reactants Reload Reagents Rcload Pathway IWorkspace Light, Peroxide Review Examples Alkene Addition Alkanes, Radical Reactions Reactions of Substituted Benzenes CH, Pathway (0.000 sec) Reactants Reagents Products Select a...
2 problems REVIEW Topics [References) CH HC OCH Br2 CH3 B H3C CH,OH H₂C CH₂ Electrophilic addition of hypohalous acids to alkenes yields a 1,2-haloalcohol called a halohydrin. Halohydrin formation, however, does not result from the addition of HOBr, for example. Instead the addition is done indirectly by reaction of the alkene with Br, in the presence of water. The reaction also works with Cl2 to give chlorohydrins instead of bromohydrins. The reaction proceeds through a cyclic intermediate known as...