1. Phenylmagnesium bromide undergoes many different reactions. complete the following equation to show the expected products:...
1. Phenylmagnesium bromide undergoes many different reactions. complete the following equation to show the expected products:
2. Grignard reactions are often used to prepare alcohol. Many
times the alcohols are then used to prepare other classes of
compounds. show how the following synthesis can be carried out
using grignard reactions followed by additional steps.
Homework Answers
Given below are the detailed reaction schemes for 1. a) to e) and synthetic procedures for 2. a) and 2. b) two methods in case of b for the formation of the final product.
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1. Phenylmagnesium bromide undergoes many different reactions.
complete the following equation to show the expected products:...
Write the product and a complete arrow-pushing mechanism and propose (the) major product(s) for the following...
Write the product and a complete arrow-pushing mechanism and propose (the) major product(s) for the following transformation. After a Grignard reaction. .... Each of the Grignard reactions we have studied so far produces an alcohol as the major organic product. Alcohols can be used as starting materials for a number of organic reactions. Use this exercise to consider the range of reactions that can be performed after a Grignard reaction. For each reaction sequence below, suggest a Grignard reagent and...
Problem 1. Synthesize the following alkene through the Wittig reaction of a carbonyl compound and a...
Problem 1. Synthesize the following alkene through the Wittig reaction of a carbonyl compound and a Wittig reagent. 2,3-diphenyl-2-butene 2. Predict the products of the following reactions. Casco CHCH.CHCH, CHCH.CH но ats ОО 2.0 CH,CHACHCH,CHCHOCH.CH, CH 3. A useful and general method for the synthesis of alcohols is the addition of Grignard reagents to carbonyl compounds. Show what Grignard reagent and what carbonyl compound you would start with to prepare the alcohol below. List all possibilities. 2-methyl--butanol 2-METHYL-2- BOTANIC
Show the products for the following reactions. Propose starting materials that can form the follo...
Show the products for the following reactions. Propose starting
materials that can form the following product in one step.
NaOH, Br2 d. PCls. Br2 он e. 4. Propose starting materials that can form the following product in one step Compound Z Synthesize the starting materials you proposed above from Ethanal and ethyl acetate (do not use other carbonyl compounds). You can use ethanal and ethyl acetate as many times as you need to. Hint: you will use the 3 carbon-carbon...
Draw products A and B of the following series of reactions. Ethyl phenylacetate + 1. CH_3CH_2O^-,...
Draw products A and B of the following series of reactions. Ethyl phenylacetate + 1. CH_3CH_2O^-, followed by aq. HCl rightarrow Product A Product A + aq. HCl, heat rightarrow Product B (Phenylacetic acid is C_6H_5CH_2COOH) Show the steps that make 2-methyl-3-phenylpropanoic acid by the malonic ester synthesis.
Provide expected products of each of the following reactions featuring 1-phenylpropanone OEt LDA base propyl bromide...
Provide expected products of each of the following reactions
featuring 1-phenylpropanone
OEt LDA base propyl bromide H2, Rh н.с CH Mg Br HNO Hso4 SO3 SH Raney Nic H2S04 Ph base LiAlH PC Ph Ph CH NO
1. Predict the major products formed when benzene reacts with the following reagents. (a). tert-butyl bromide,...
1. Predict the major products formed when benzene reacts with the following reagents. (a). tert-butyl bromide, ALCl3 (b) bromine + a nail (c) iodine + HNO3 (d) carbon monoxide, HCl, and AlCl3/CuCl (e) nitric acid + sulfuric acid. 2. Predict the major products of the following reactions. (a.) nitrobenzene + ethyl chloride/AlCl3 (b). p-methylanisole + acetyl chloride + AlCl3 (c). nitrobenzene + fuming sulfuric acid (d) benzene + CH3CH2COCl in the presence of (1) ALCl3 followed by...
Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepa...
i need help with the prelab questions please
Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepare a Grignard reagent, phenyl magnesium bromide, from bromobenzene and magnesium metal. The Grignard reagent will then react with methyl benzoate to form triphenylmethanol. Introduction Grignard reagents, such as organomagnesium halides, were discovered in 1910 by French chemist Victor Grignard. The Grignard reaction is one of the most general methods for carbon- carbon bond formation in all of organic chemistry....
Grignard Reaction 1. Draw your complete reaction, including the formation of the Grignard reagent and the...
Grignard Reaction 1. Draw your complete reaction, including the formation of the Grignard reagent and the reaction with your carbonyl compound. Below each reagent, write its molecular weight and density (if a liquid). Also write how much of each material you will use in ml (if liquid), grams, and moles. Also include the molecular weight and melting point of your final product. 2. How many moles of Grignard reagent are you synthesizing? What mass of water could fully react with...
Complete questions 10-27 PART II: REACTIONS: Here is another different" question. Pretend you have been asked...
Complete questions 10-27
PART II: REACTIONS: Here is another different" question. Pretend you have been asked by me to put together a bunch of one-step reactions WITH starting materials (your choice), reagents and answers to help me with writing a final exam. For example: let's say I ask you to give an example of a free radical chlorination with a non-cyclic compound. Below would be your answer. As I am pretty sure you can figure out, there are millions of...
Help sos 1. Show the expected product(s) of the following reactions. For products containin or cis/trar...
Help sos
1. Show the expected product(s) of the following reactions. For products containin or cis/trar asymmetric carbon atoms, indicate relative stereochemistry (syn/anti relationships) and/or whether a racemic mixture is produced. (8 pts each) 1. HNO3, H2so4 NO 2. Fe, HCI OCH3 3. NaNO2 aq. HCI 4, CuCN, Δ сно но 1. Br2 H20 2. Fe SO)S b. HO- -H OH s CH2OH 1. SOCI2 2. NH3 H3C 3. Br2 NaOH, H2O 1. KOH 2. PhCH2CH Br 3. NH2NH2 d....
Write the product and a complete arrow-pushing mechanism and propose (the) major product(s) for the following transformation. After a Grignard reaction. .... Each of the Grignard reactions we have studied so far produces an alcohol as the major organic product. Alcohols can be used as starting materials for a number of organic reactions. Use this exercise to consider the range of reactions that can be performed after a Grignard reaction. For each reaction sequence below, suggest a Grignard reagent and...
Problem 1. Synthesize the following alkene through the Wittig reaction of a carbonyl compound and a Wittig reagent. 2,3-diphenyl-2-butene 2. Predict the products of the following reactions. Casco CHCH.CHCH, CHCH.CH но ats ОО 2.0 CH,CHACHCH,CHCHOCH.CH, CH 3. A useful and general method for the synthesis of alcohols is the addition of Grignard reagents to carbonyl compounds. Show what Grignard reagent and what carbonyl compound you would start with to prepare the alcohol below. List all possibilities. 2-methyl--butanol 2-METHYL-2- BOTANIC
Show the products for the following reactions. Propose starting
materials that can form the following product in one step.
NaOH, Br2 d. PCls. Br2 он e. 4. Propose starting materials that can form the following product in one step Compound Z Synthesize the starting materials you proposed above from Ethanal and ethyl acetate (do not use other carbonyl compounds). You can use ethanal and ethyl acetate as many times as you need to. Hint: you will use the 3 carbon-carbon...
Draw products A and B of the following series of reactions. Ethyl phenylacetate + 1. CH_3CH_2O^-, followed by aq. HCl rightarrow Product A Product A + aq. HCl, heat rightarrow Product B (Phenylacetic acid is C_6H_5CH_2COOH) Show the steps that make 2-methyl-3-phenylpropanoic acid by the malonic ester synthesis.
Provide expected products of each of the following reactions
featuring 1-phenylpropanone
OEt LDA base propyl bromide H2, Rh н.с CH Mg Br HNO Hso4 SO3 SH Raney Nic H2S04 Ph base LiAlH PC Ph Ph CH NO
i need help with the prelab questions please
Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepare a Grignard reagent, phenyl magnesium bromide, from bromobenzene and magnesium metal. The Grignard reagent will then react with methyl benzoate to form triphenylmethanol. Introduction Grignard reagents, such as organomagnesium halides, were discovered in 1910 by French chemist Victor Grignard. The Grignard reaction is one of the most general methods for carbon- carbon bond formation in all of organic chemistry....
Grignard Reaction 1. Draw your complete reaction, including the formation of the Grignard reagent and the reaction with your carbonyl compound. Below each reagent, write its molecular weight and density (if a liquid). Also write how much of each material you will use in ml (if liquid), grams, and moles. Also include the molecular weight and melting point of your final product. 2. How many moles of Grignard reagent are you synthesizing? What mass of water could fully react with...
Complete questions 10-27
PART II: REACTIONS: Here is another different" question. Pretend you have been asked by me to put together a bunch of one-step reactions WITH starting materials (your choice), reagents and answers to help me with writing a final exam. For example: let's say I ask you to give an example of a free radical chlorination with a non-cyclic compound. Below would be your answer. As I am pretty sure you can figure out, there are millions of...
Help sos
1. Show the expected product(s) of the following reactions. For products containin or cis/trar asymmetric carbon atoms, indicate relative stereochemistry (syn/anti relationships) and/or whether a racemic mixture is produced. (8 pts each) 1. HNO3, H2so4 NO 2. Fe, HCI OCH3 3. NaNO2 aq. HCI 4, CuCN, Δ сно но 1. Br2 H20 2. Fe SO)S b. HO- -H OH s CH2OH 1. SOCI2 2. NH3 H3C 3. Br2 NaOH, H2O 1. KOH 2. PhCH2CH Br 3. NH2NH2 d....
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