Suggest a synthesis for the following alcohol starting from an aldehyde or ketone and 1-propenylmagnesium bromide.<img src="//img.wizedu.com/questions/2b2040c0-d058-11ec-af7c-190795bedca4.png" title="1652183745105060.png" alt="image.png"/>

Question

In: Chemistry

Suggest a synthesis for the following alcohol starting from an aldehyde or ketone and 1-propenylmagnesium bromide....

Suggest a synthesis for the following alcohol starting from an aldehyde or ketone and 1-propenylmagnesium bromide.

Solutions

Expert Solution

queen_honey_blossom answered 1 year ago

Next > < Previous

Related Solutions

Choose a compound that is classified as an ether, aldehyde, ketone, ester, or alcohol. Report on...

Choose a compound that is classified as an ether, aldehyde, ketone, ester, or alcohol. Report on how this compound is used. Can you find a way in which the structure of your molecule influences it's function? Next, write the condensed structural formula of a simple molecule with an ether, aldehyde, ketone, ester, or alcohol functional group for your peers to name. Then, determine the name of one of the molecules that your peers posted, walking us through the naming process.

a) Why does the ketone (1-indanone) react with the base, but the aldehyde (3,4- dimethoxybenzaldehyde) does...

a) Why does the ketone (1-indanone) react with the base, but the aldehyde (3,4- dimethoxybenzaldehyde) does not? b) Why is the α-proton so acidic? (You must support your argument with appropriate drawings).

Suggest a procedure to convert 1-hexene to the other alcohol you did not obtain from this...

Suggest a procedure to convert 1-hexene to the other alcohol you did not obtain from this experiment. (not 1-hexanol) Briefly: a. Provide a balanced equation b. Outline a brief reaction procedure – what solvent, temperature and conditions should be used? What glassware? c. How would you separate the product from the reaction mixture? d. How would you determine the identity and purity of the product?

Make a flow chart for the synthesis of Benzoic Acid from phenyl magnesium bromide and carbon...

Make a flow chart for the synthesis of Benzoic Acid from phenyl magnesium bromide and carbon dioxide. Using your knowledge of the physical properties of the solvents, reactants, and products, show how the products can be purified. Indicate which layer should contain the product in the liquid/liquid extraction steps.

The experiment to get Isoamyl Bromide from Isoamyl Alcohol was done. chemicals used were: 9 grams...

The experiment to get Isoamyl Bromide from Isoamyl Alcohol was done. chemicals used were: 9 grams (.087 moles) of sodium bromide, 8.2 mL (6.6 grams; .075 moles) of isoamyl alcohol, 8mL (14.7 grams;.150 moles) of concentrated sulfuric acid, and 8mL of 10% aqueous sodium carbonate. What are the limiting reagents? What is the theoretical yield? What is the % yield?

ORGANIC CHEMISTRY experiment : Synthesis of n-butyl bromide (Sn2) 1.what is the function of the Hickman...

ORGANIC CHEMISTRY experiment : Synthesis of n-butyl bromide (Sn2) 1.what is the function of the Hickman Still in this experiment? 2. what is the function of the condenser in this experiment?

give the steps for the enantioselective synthesis of (L)-tyrosine and another for (D)-tyrosine both starting from...

give the steps for the enantioselective synthesis of (L)-tyrosine and another for (D)-tyrosine both starting from the corresponding (Z)-enamido acid and using a rhodium as a catalyst

Sodium Borohydride Reduction of a Ketone 1. How will the dibenzalacetone product be isolated from the...

Sodium Borohydride Reduction of a Ketone 1. How will the dibenzalacetone product be isolated from the reaction mixture and how will it then be further purified? How will the product be characterized? 2. What apparatus and conditions (solvent, temp., reaction time, etc) will be used for the reaction? 3. Identify which is the reducing agent and which is the oxidizing agent in the reaction of benzophenone with sodium borohydride and explain your reasoning, ie. show the changes in oxidation states...

Devise a synthesis of 5-methyl-1-hexyne using one of the starting materials and any of the reagents...

Devise a synthesis of 5-methyl-1-hexyne using one of the starting materials and any of the reagents below using the fewest steps possible. If you need fewer than the 3 steps allowed, enter "none" for reagents in the remaining unused steps. Starting Materials: (1.) HC(triple bonded)CH (2.) HC(triple bonded)C-CH3 (3.) HC(triple bonded)C-CH2CH3 (4.) HC(triple bonded)C-CH2CH2CH2CH3 (5.) HC(triple bonded)C-CH(CH3)(CH3) (6.) HC(triple bonded)C-C(CH3)(CH3)(CH3) Reagents: a. NaNH2/NH3 (l) b. NaOH/H2O c. iodomethane d. idoethane e. 1-bromopropane f. 2-bromopropane g. 1-bromo-3-methylbutane h. t-butyl bromide i....

Mutliple step synthesis for 4-bromoacetanilide from aniline 1. during the synthesis of aniline from nitrobenxe, explain...

Mutliple step synthesis for 4-bromoacetanilide from aniline 1. during the synthesis of aniline from nitrobenxe, explain why it was necessary to make the solution alkaline (addition of NaOH) 2. During filtration, why is it important to only wash the solid with ice-cold solvent? 3. Why is it necessary ti acylate aniline prior to bromination? 4. If the synthesis of p-bromoacetanilide also provided a small amount of o-bromoacetanilide after the crystallixation step, how would that influence the melting point range od...

Subjects