For the reaction below: a Draw the structure of the major organic product. (Do not include diisopropylamine.) Move Clear Erase Undo Redo Increase Scale Decrease Scale Copy Paste Set Label More Labels Attributes More Attributes Single Bond Recessed Bond Protruding Bond Double Bond Other Bond More Bonds Cyclohexane Ring Benzene Ring Other Ring More Rings Bracket Correct Owing to the high basicity of the enolate nucleophile, this alkylation is practical only with methyl and primary alkylating agents. For secondary and tertiary substrates, E2 elimination is the favored pathway. Multiple alkylation can be a significant side reaction. b Write the mechanism of the following reaction step using curved arrows to show electron reorganization.

This element exists in adundance in the sun.explain how you would go about capturing sunlight.would this captured sunlight contain any of the element?

What is the percentage composition of carbon in the compound ch4

Which explanation is true about what happens to a ray of light when it strikes a mirror? a. a light ray is transmitted toward a mirror at a certain angle. the light ray is then reflected by the mirror at an equal angle but in the opposite direction of the transmitted ray. b. an incident ray strikes a mirror at an angle with a line perpendicular to the mirror. the light ray is then reflected at an angle equal to the angle of incidence but on the opposite side of the perpendicular line. c. a reflecting ray strikes a mirror at an angle with a line perpendicular to the mirror. the light ray is then refracted at an angle equal to the angle of the reflecting ray and on the same side of the perpendicular line. d. an incident ray strikes a mirror at an angle with a line parallel to the mirror. the light ray is then transmitted at an angle equal to the angle of incidence but on the opposite side of the parallel line. you so much! : -d take the time to try and answer correctly.