Video Solution: Specify reagents suitable for converting 3-ethyl-2-pentene t...

Sign up for free to keep watching this solution

Specify reagents suitable for converting 3-ethyl-2-pentene to each of the following:

(d) 3-Ethyl-3-pentanol 

Predict the organic product(s) for the following reaction. Be sure to indicate stereochemistry when appropriate, if stereoisomers are produced draw one and state the relationship between the other stereoisomer formed. (enantiomers, diastereomers, etc.).

Watch Solution

Give three examples of acid-catalyzed reactions. For each example clearly indicate the starting material, reagents and products.

Watch Solution

The acid catalyzed addition of water to alkenes is a common method to prepare alcohols. For the example below, show the mechanism of this reaction. Include all flows of electrons, charges and intermediates. The mechanism MUST show how the acid is catalytic. 

Watch Solution

Please provide the full arrow-pushing mechanism for this reaction. Include stereochemistry for the final product if applicable. 

Watch Solution

Which of the following molecules would be produced from the reaction below?

Watch Solution

Illustrate the mechanism for the following reaction. Indicate all arrows and structures of intermediates.

Watch Solution

The following problems are a new format. We turn the tables and give you the product. In the space provided show the starting material required to make that product using the given reagents. When more than one starting material would work, you must draw both.

Watch Solution

Create the full arrow pushing mechanism which shows all intermediates and all products that result from these reactions and label minor and major products if they are not equal in potential energy.

Watch Solution

Draw the starting material that under the given reaction conditions, result in the following product.

Watch Solution

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. 

Watch Solution

Follows Markovnikov’s Rule

a)  Hydrogen goes to the double bonded carbon with _______ hydrogens. ( ______ substituted alkene carbon) 

b)    Hydroxide ion goes to the ___________ stable carbocation

 

Watch Solution

Write a mechanism for the following reaction.

Watch Solution

Predict the product(s) or reagents of the following reactions.

Watch Solution

The acid catalyzed addition of water to alkenes is a common method to prepare alcohols. For the example below, show the mechanism of this reaction. Include all flows of electrons, charges and intermediates. The mechanism MUST show how the acid is catalytic.

Watch Solution

How many atoms and electrons are directly involved in the bond-making and bond-breaking of the reaction given below?  Choose the right answer. 

The first step of hydronium ion-catalyzed addition of water to an alkene

a) four atoms, four electrons

b) four atoms, three electrons

c) four atoms, two electrons

d) three atoms, four electrons

e) three atoms, three electrons

f) three atoms, two electrons 

g) two atoms, three electrons

h) two atoms, two electrons

Watch Solution

Identify the nucleophile that attacks the carbocation intermediate in the acid-catalyzed hydration shown. 

Watch Solution

What is the major product from the reaction shown?

Watch Solution

Provide a detailed mechanism for the following reaction using a curved arrow notation.

Watch Solution

Provide a detailed mechanism for the following reaction using a curved arrow notation. 

Watch Solution