CH3 CH3 - H2O elimination Draw Intermediate a (CH3)2NH Deprotonati on Draw Product

Which carbocation is the most stabilized? Me Me CO₂Me MeO A B C D Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. a A b B CC OMe Me Me OMe Me Me MeO. OMe E Me Me

What is the product? SH CH3O Na CH3OH Na + CH3OH Na + CH3OH -0-CH +CH3OH

When 1-butene reacts with HBr the reaction mechanism proceeds through a? secondary carbocation bromonium ion tertiary carbocation O There is no intermediate formed since the reaction is concerted primary carbocation

Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. CH3 CH3 H3PO4 HO, + H3C CH3 HO HO First stage in synthesis of the epoxy and polycarbonate ingredient bisphenol-A You do not have to consider stereochemistry. Include all valence lone pairs in your answer. In cases where there is more than one answer, just draw one.

Fill in the missing products and intermediates

Draw the arrow pushing mechanisms and product

Draw the products for the reaction. Include both the major organic product and the inorganic product. If more than one stereoisomer is possible, draw only one stereoisomer. Include stereochemistry where relevant.

Draw the product of the oxidation of the given aldehyde. Include all hydrogen atoms. H3C-CH₂-CH₂-CH-CH₂-CH₂-CH3 oxidation -H What is wrong with this Incorrect U OH k H₂ H₂C -(-CC-CC H₂ H₂ H H₂ O

Which of the following is most polar? CH3CH2OH CH3CH2CH2CH2CH2OH CH3OH CH3CH2CH2CH2OH