Chem 1 7. Provide each of the following alkene-containing molecules with acceptable names. Be careful to...
oChem 1 7. Provide each of the following alkene-containing molecules with acceptable names. Be careful to assign the configurations of any chiral centers (R or S) and double bonds (E or Z).
OChem 1 7. Provide each of the following alkene-containing molecules with acceptable names. Be careful to assign the configurations of any chiral centers (R or S) and double bonds (E or Z). b. Br Br
1. Provide each of the followine alkhalides with acceptable names. You may use either the new ctional class of wha v e nomenclature as appropriate. Be sure to assign the configurations of any chiral Center (30, 73, 8e) -7-chloro-3-fluno - 44, 8. trimethyldecane GR)-6 diflouro-7-ethyl-2-methyl underane 1,3,5R 63, 42)-2-4-dimell o)--chloss house, sx) -1- Crono-s-bet1:30 meth/propy eyelheme 4- Toyclopentane 2. Draw detailed mechanisms for the following reactions that use "curved arrows" to show the breaking and forming of bonds and identify...
8. Draw detailed mechanisms for the following reactions that use "curved arrows" to show the breaking and forming of bonds and identify the mechanism that is operating. a HEC Br CH3 OH NaOCH H2SO + HOCH NHE + H₂O heat KOB HAPO + HOB + KCI •H₂O THE heat 9. Provide the products expected to be formed under each of the following sets of conditions. a. HO CHI H2SO4 NaOCH LIOCH heat THE DMSO кожи ETOH heat THF
1-24 need help really lost Proton Transfer: deprotonation D. 1) Add the appropriate curved arrows for the following deprotonation step. Also add the other product notice how the Tema s can be converted to this by use of a strong base such as sodium a sodium ion (Na) is not drawn, in this case it is just a spectatorio PCW27 - Mechanistic steps - Part Name: Time spent 2) Label the above compounds with the appropriate name from the previous...