Question

Draw the mechanism for the ozonolysis of an alkene. Draw the necessary starting material to produce...

Draw the mechanism for the ozonolysis of an alkene. Draw the necessary starting material to produce acetone and acetaldehyde. Name this alkene starting material

Homework Answers

Answer #1

Solution :

Ozonolysis of alkene produces aldehydes and ketones. The mechanism is completed via formation of an unstable triozonide which on further converted into corresponding aldehydes and ketones.

The mechanism of ozonolysis of alkene is given below.

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
Draw the mechanism for addition of Br2 to an alkene.
Draw the mechanism for addition of Br2 to an alkene.
What is the alkene hydration mechanism for the product 2,3-Dimethyl-2-butanol, the starting materials are 3,3-Dimethyl-1-butene, water,...
What is the alkene hydration mechanism for the product 2,3-Dimethyl-2-butanol, the starting materials are 3,3-Dimethyl-1-butene, water, sulfuric acid (H2SO4)? Please draw out details with an explanation!
What is the mechanism for Alkene Dihydroxylation reaction of cis-octahydro-naphthalene-4a,8a-diol, the starting materials are 1,2,3,4,5,6,7,8-Octahydro-naphthalene and...
What is the mechanism for Alkene Dihydroxylation reaction of cis-octahydro-naphthalene-4a,8a-diol, the starting materials are 1,2,3,4,5,6,7,8-Octahydro-naphthalene and OsO4?
Use the Marvin editor to draw the skeletal structures of the starting material and the major...
Use the Marvin editor to draw the skeletal structures of the starting material and the major organic product given the following: 1) The reagent is HCl at room temperature. 2) The proton NMR spectrum for the starting material is given below. 3) The integration data gives a relative ratio (in decreasing ppm order) of 1:4:3:6. A) Starting material. B) MOP
1-The starting alkene has a boiling point of 102C and the product alcohol has a boiling...
1-The starting alkene has a boiling point of 102C and the product alcohol has a boiling point of 137C. What will be the order of elution for the starting material and the product if you ran a GC on an incomplete reaction? 2- Is the product of the reaction chiral? How many stereoisomers will be produced? Is the product of the reaction optically active?
Draw the mechanism for the elimination of the product from Question #2 (written below) using KOH...
Draw the mechanism for the elimination of the product from Question #2 (written below) using KOH and heat. The first elimination follows a classical E2 mechanism and the product is an alkene with the phenyl groups in a cis configuration. Since the bromine and hydrogen are not in an anti-coplanar arrangement, the second elimination cannot proceed through an E2 mechanism. Instead it is said to proceed through an E1cB mechanism. Question 2 for reference: Draw the mechanism for the bromination...
Draw the full mechanism of the crossed aldol condensation reaction of 4-chlorobenzaldehyde with acetone. (There are...
Draw the full mechanism of the crossed aldol condensation reaction of 4-chlorobenzaldehyde with acetone. (There are 2 equivalents of 4-chlorobenaldehde and 1 equivalent of acetone and the product is 1,5-bis(4-chlorophenyl)-1,4-pentadien-3-one).
Draw the reaction mechanism for the synthesis of methyl diantilis from 3-ethoxy-4-hydroxybenzaldehyde. Use NaOH/NaBH4 to produce...
Draw the reaction mechanism for the synthesis of methyl diantilis from 3-ethoxy-4-hydroxybenzaldehyde. Use NaOH/NaBH4 to produce 3-ethoxy-4-hydroxybenzyl alcohol first. Then use Amberlyst-15/1-propanol to produce the methyl diantilis. Include the mechanism for the reduction of NaBH4.
Using 2-propanol, or rubbing alcohol, as your only starting material, draw a path of synthesis (with...
Using 2-propanol, or rubbing alcohol, as your only starting material, draw a path of synthesis (with structures, reagents, and solvents) that would deliver 2,3-dimethyl-butan-2-ol using Grignard reagent.
Alkene Hydration LAB 3.    Choose the starting materials: styrene, and water, which is the solvent. 4.    Return to...
Alkene Hydration LAB 3.    Choose the starting materials: styrene, and water, which is the solvent. 4.    Return to the lab and build the experiment apparatus, which includes a heater, condenser, nitrogen gas. 5.    Add the reagent, sulfuric acid (H2SO4) to the reaction flask. 6.    You will monitor the reaction progress using the pull down TV and TLC. QUESTION 1 The product produce when styrene is reacted with sulfuric acid in the presence of water is a. benzoic acid b. phenol c. 1-phenylethanol d. 2-phenolethanol...