Draw structural formulas for the a,ẞ-unsaturated aldehyde or ketone and the lithium diorganocuprate (Gilman reagent) that could be used in a synthesis of the compound shown below. . You do not have to consider stereochemistry. . In cases where there is more than one answer, just give one. . If a structure has a copper-lithium bond, draw the lithium ion in a separate sketcher. ⚫ Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. ⚫ Separate multiple reactants using the + sign from the drop-down menu. ? 0 -> ? 34 -
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- Draw structural formulas for the a,ß-unsaturated aldehyde or ketone and the lithium diorganocuprate (Gilman reagent) that could be used in a synthesis of the compound shown below. oly O • You do not have to consider stereochemistry. • In cases where there is more than one answer, just give one. • If a structure has a copper-lithium bond, draw the lithium ion in a separate sketcher. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple reactants using the + sign from the drop-down menu. *** ? #[ ] درDraw structural formulas for the a,ß-unsaturated aldehyde or ketone and the lithium diorganocuprate (Gilman reagent) that could be used in a synthesis of the compound shown below. You do not have to consider stereochemistry. • In cases where there is more than one answer, just give one. • If a structure has a copper-lithium bond, draw the lithium ion in a separate sketcher. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple reactants using the + sign from the drop-down menu. . 89 4 Sa FDraw structural formulas for the a,ß-unsaturated aldehyde or ketone and the lithium diorganocuprate (Gilman reagent) that could be used in a synthesis of the compound shown below. O CH3 H a • You do not have to consider stereochemistry. • In cases where there is more than one answer, just give one. • If a structure has a copper-lithium bond, draw the lithium ion in a separate sketcher. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu i the bottom right corner. Separate multiple reactants using the + sign from the drop-down menu. $3 -85 • Sn [1
- Draw structural formulas for the a,ß-unsaturated aldehyde or ketone and the lithium diorganocuprate (Gilman reagent) that could be used in a synthesis of the compound shown below. You do not have to consider stereochemistry. In cases where there is more than one answer, just give one. If a structure has a copper-lithium bond, draw the lithium ion in a separate sketcher. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple reactants using the + sign from the drop-down menu. • 0 Call ? [FDraw structural formulas for the a,ß-unsaturated aldehyde or ketone and the lithium diorganocuprate (Gilman reagent) that could be used in a synthesis of the compound shown below. H3C. You do not have to consider stereochemistry. • In cases where there is more than one answer, just give one. If a structure has a copper-lithium bond, draw the lithium ion in a separate sketcher. •Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. •Separate multiple reactants using the + sign from the drop-down menu. ? [P ChemDoodle Previous Next>Draw structural formulas for an aldehyde or ketone and alkyl (or aryl) bromide that could be used in a Grignard synthesis of the alcohol shown OH CHCH,CH,CH3 • You do not have to consider stereochemistry. If there is more than one combination, draw only one Draw one structure per sketcher, Add additional sketchers using the drop-down menu in the bottom right corner. Separate multıple reactants using the sign from the drop-down menu.
- Draw structural formulas for the a,ß-unsaturated aldehyde or ketone and the lithium diorganocuprate (Gilman reagent) that could be used in a synthesis of the compound shown below. OCH2CH3 You do not have to consider stereochemistry. In cases where there is more than one answer, just give one. • If a structure has a copper-lithium bond, draw the lithium ion in a separate sketcher. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate multiple reactants using the + sign from the drop- down menu.Draw structural formulas for the a,ß-unsaturated aldehyde or ketone and the lithium diorganocuprate (Gilman reagent) that could be used in a synthesis of the compound shown below. You do not have to consider stereochemistry. • In cases where there is more than one answer, just give one. If a structure has a copper-lithium bond, draw the lithium ion in a separate sketcher. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple reactants using the + sign from the drop-down menu. ● ● FULL ? Ⓡ ChemDoodle Sn [FDraw a structural formula of an alkene or alkenes (if more than one) that undergo acid-catalyzed hydration and without rearrangement give 1-methylcyclohexanol as the major product. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • If more than one structure fits the description, draw them all. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate structures with + signs from the drop-down menu. ● AAVII -85 ? ChemDoodleⓇ Y [F
- The conversion of alcohols into alkyl halides by reaction with hydrogen halides is an example of a Nucleophilic Substitution Reaction. This kind of reaction can proceed by two different mechanisms depending on the structure of alcohol substrates used. Generally, primary alcohols are substituted via SN2 mechanism, while secondary and tertiary alcohols undergo SN1 mechanism. Consider the following reaction given in the picture below and the questions in the picture too.Draw structural formulas for the a B-unsaturated aldehyde or ketone and the lithium diorganocuprate (Gilman reagent) that could be used in a synthesis of the compound shown below. • You do not have to consider stereochemistry. • In cases where there is more than one answer, just give one. If a structure has a copper-lithium bond, draw the lithium ion in a separate sketcher. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple reactants usıng the sign from the drop-down memu.4. A certain endothermic reaction X carried out room temperature (273K) has an enthalpy change of 20 Kcal/mol and an entropy change of 10 Kcal/K/mol. i) Calculate the Gibbs free energy (AG) of this reaction. ii) Is this reaction spontaneous or non-spontaneous? Give a reason for your answer 5. Thiomethane reacts with compound A via an SN1 reaction. Complete its reaction equation below. ii) SH Compound A ii) Draw the mechanism of reaction for this reaction. 6. Butyl Chloride undergoes an elimination reaction when reacted with sodium ethoxide to form butene. The reaction equation is given below with two reaction products A and B. low inevloa CI noitsups p *OEt B Which is the major product, and which is minor product. (Hint: Look up how the size of the base affects the elimination reaction product) Give a reason for your answer.