Predict the organic product(s) of the following reaction. When appropriate, be sure to indicate stereochemistry. If more than one product is formed be sure to indicate the major product, if stereoisomers are produced in the reaction be sure to indicate the relationship between them. Draw the answer in skeletal form.
Which of the following would be a reasonable synthesis of CH 3CH2CH2CH2OH?
The principal organic product of the following transformation is: Anti-Markovnikov
In a hydroboration-oxidation reaction, a hydrogen and an alcohol are added where there once was a double bond. Describe the regio- and stereochemical relationship between the two.
For the transition state structure below, choose an organic reaction in which it is involved and give a chemical equation for your selected organic reaction that includes the following:
(i) structural formula(s) for the organic reactant(s); be sure to show stereochemistry appropriately when necessary
(ii) the experimental conditions (Give structural formulas for organic compounds. Give a chemical formula or inorganic reactants or catalysts . If heat and/or light is needed, be sure to indicate it appropriately.)
(iii) structural formula(s) for the major organic product(s); be sure to show stereochemistry appropriately when necessary. As we do for most organic reaction equations, the chemical equations that you give do not need to be balanced.
Provide the following when a product is given. If an organic reactant is missing, supply a structural formula; if an inorganic reactant (reagent) or catalyst is missing, simply give a formula.
Supply the missing inorganic reactant (reagent) or catalyst that is missing in the reaction given below.
Draw the starting material that under the given reaction conditions, result in the following product.
Fill in the box with the product of the following reaction of alkenes. Draw only the PREDOMINATE REGIOISOMER and indicate stereochemistry by drawing dashes and wedges where appropriate. When a racemic mixture is formed you must draw both enantiomers and write RACEMIC in the box.
Fill in the box with the product of the following reaction of alkene. Assume that the starting alkene is enantiomerically pure and optically active. Draw only the PREDOMINATE REGIOISOMER and indicate stereochemistry by drawing dashes and wedges where appropriate. In the box label the product as “optically active” or “optically inactive”.
Show how you would carry out each of the following reactions. You do NOT need to draw the mechanisms
Follows Anti-Markovnikov’s Rule
a) Hydrogen goes to the double bonded carbon with _______ hydrogens. ( ______ substituted alkene carbon)
b) Hydroxide ion goes to the double bonded carbon with _______ hydrogens. ( ______ substituted alkene carbon).
Give the product, or products, including stereochemistry of the reaction of (Z)-3-methyl-2-pentene with the reagent below. If the products are a pair of enantiomers, you need to draw only one and state that the other enantiomer is formed.
BH3, THF - H2O/H2O2, NaOH
Predict the starting material of the following reactions.
Predict the product(s) or reagents of the following reactions.
Predict the product for the reaction below.
Predict the major product of the reaction shown.
Complete the following reaction with the correct structure of the product. Don’t forget to specify the stereochemistry.
What will be the major product of the following reaction? Pay careful attention to the stereochemistry of the product.
Which of the following would be produced from the following reaction?
a) 1 and 4
b) 1, 2, 3, and 4
c) 3 and 4
d) 2 and 3
e) 1 and 2
Give all possible product/products and designate stereoselectivity &/or regioselectivity by using wedges and dashes.
Determine the mechanism and predict the product of the reaction: