3). Provide products of the following Diels-Alder reactions (include stereochemistry) 4). What starting material would be necessary to prepare the following compound by Diels-Alder reaction?
Include arrows and all steps
What are the products for the following nucleophilic substitution reaction: OCH3 30 H2CO CH2CH2CH2CH2OH 1. TsCI, Pyridine 2. Lil, Acetone H3CO
2. (8 pt) Part A. Give conditions that could be used to catalyze the equilibrium reaction below, and show a complete mechanism. Will the equilibrium favor the reactants or products, and why? OH
B only please
6| What products would you expect to obtain from reaction of 1-methylcyclohexanol with the following reagents? a) HBO b) Na2Cr2O7 (oxidizing agents)
Draw a structural formula for the organic product of the following acid catalyzed reaction. benzaldehyde + hydroxylamine →
You do not have to consider stereochemistry.
Do not draw organic or inorganic by-products.
I0 I. Suggest a synthetic route. Clearly show all intermediates (i.e intermediate products) and reaction conditions. 0 TOH hea + び. hemi Ketal acetal
Conceptual Checkpoint 20.12
Draw all the product(s) for each reaction below. If there are
two identical molecules among products, draw each of them.
Incorrect. OH Edit
2) Explain why the esterification reaction of carboxylic acids with bulky alcohols(eg tBuOH) does not generate products. What would be an alternative method to obtain these esteres? esters
1. draw the curved arrow mechanism for the reaction of propene with br2 in excess water. draw and name products 2. draw the structure for (E) -4-bromohepta-1,3-diene?
Calculate the distribution of the products according to the probability and reactivity of the chlorination reaction of the irradiated 2,3-dimethylpentane with ultraviolet light. (tertiary speed rate: 5.0, secondary: 3.8, primary = 1.0)