1. For each molecule below, draw the most stable enolate that forms upon reaction with NaOH....
Use Office Lens to scan your assignment ID Number: Section: 1. For each molecule below, draw the most stable enolate that forms upon reaction with NaOH. 2. When a combination of acetaldehyde and propanal is treated with aq. NaOH, four B-hydroxyaldehydes form. (a) Draw the products, neglecting stereochemical indicators. (b) For each product, determine the number of stereoisomers present. two products with the same m.w. product with smallest m.w. product with largest m.w. • NaOH # of 1 stereo-1 isomers...
Draw the enolate ion that is formed when the following molecule is treated with NaOH. Draw the resonance structures of the enolate. Draw the products formed in the following reactions
Draw the two resonance structures that most accurately describe the enolate that forms when the aldehyde below is treated with sodium hydroxide.
Draw most stable chair form for the more stable stereoisomer for the molecule. All help is appreciated yclohexane Chair Practice 9. For each of the following do two things: A draw the most stable chair form for the more stable stereoisomer for the molecule B. identify whether the more stable stereoisomer is cis or trans. 7. 1-butyl-2-methylcyclohexane 8. 3-t-butyl-1-methylcyclohexane 9. 1,4-diethylcyclohexane C. For each of the following, do two things: A draw the most stable chair form over groups C...
2. Draw the most stable conformer of each molecule. Emphasize the stability of each molecule through Newman Projections.
(9 points) 1. In each case, draw all reasonable resonance forms. Circle the most stable (plus any ties). (a) (b) (1 pt) 2. For the following Diels-Alder reaction, label the Endo and Exo products. Circle the major product.
(9 points) 1. In each case, draw all reasonable resonance forms. Circle the most stable (plus any ties). (а) o CH3-N CH3 CH3 (b) (c) (1 pt) 2. For the following Diels-Alder reaction, label the Endo and Exo products. Circle the major product Н CO2CH3 .CO2CH3 + + CO2CHS н
We also have to tell the most stable molecule for each reaction below. Can you also include that? Thank you! In which of the following reactions does the equilibrium favor the right side? Explain based on structural principles (which charged species are most/least stable?) and describe how pKa differences for the acids on either side of the equation reflect those structural principles.
(6) 5. Draw three resonance structures for the enolate of Meldrum's acid (shown below) that forms when one equivalent of NaOet is used. =1-H NaO
Draw the most stable chair conformation for the following molecule