Ch222
Select the organic STARTING material (in the context of our study thus far) that is used with Br2
Alkane
Select the reagent needed for a practical reaction with an isoalkane with more than 4 carbons.
Br2
Select the reagent needed for a practical reaction with a primary alcohol without having to heat the reaction to a high temperature.
PBr3
Select the organic STARTING material (in the context of our study thus far) that is used with PBr3
Primary Alcohol
Select the major organic PRODUCT (in the context of our study thus far) that results from the use of PBr3
Primary Alcohol Bromide
Select the organic STARTING material (in the context of our study thus far) that is used with HCl
Tertiary Alcohol
Select the major organic PRODUCT (in the context of our study thus far) that results from the use of HCl.
Tertiary Alcohol Chloride
Select the major organic PRODUCT (in the context of our study thus far) that results from the use of Br2 (provided there is an alkyl branch bonded to the parent).
Tertiary Alkyl Bromide
Select the major organic PRODUCT resulting from reaction in part G.
Tertiary Alkyl Bromide
Choose the least stable alkene out of each group. 2-methylbut-2-ene, 2-methylbut-1-ene, cis-pent-2-ene
cis-pent-2-ene
Do you use wedges and dashes with a electrophilic addition of HX
no
Do you use wedges and dashes with a free radical addition of HBr
no
Do you use wedges and dashes with a hydration via electrophilic addition under aqueous acid conditions
no
Do you use wedges and dashes with a hydrogenation with a metal catalyst using protium
no
Choose the least stable alkene out of each group. pent-1-ene, 3-methylbut-1-ene, trans-pent-2-ene
pent-1-ene
What is the name for a branched cyclowhatever
prefix+yl
Do you use wedges and dashes with a hydroboration-oxidation
yes
Do you use wedges and dashes with a hydrogenation with a metal catalyst using deuterium
yes
Do you use wedges and dashes with a vicinal dihalide formation
yes
Do you use wedges and dashes with a vicinal halohydrin formation
yes
