Homework Answers
Answer:-
These questions are answered by using simple concept of organic chemistry and reactions of ketones with Grignard reagent.
The answer is given in the image,
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Which compound(s) would be an activator and an op-director? Enter all numbers in numerical order. OH...
Which compound(s) would be an activator and an op-director? Enter all numbers in numerical order. COCH3...
Which compound(s) would be an activator and an op-director? Enter all numbers in numerical order. COCH3 Br Which two starting materials can be used to prepare the compound in the box? Enter two numbers, in numerical order.
Which starting material would give the following ketone product using the Friedel Crafts acylation adidas όόόό...
Which starting material would give the following ketone product using the Friedel Crafts acylation adidas όόόό Which two starting materials can be used to prepare the compound in the box? Enter two numbers, in numerical order. O Trieu
Practice ACS questions: Choose the compound which would be insoluble in aq. sodium hydroxide solution. а)...
Practice ACS questions:
Choose the compound which would be insoluble in aq. sodium hydroxide solution. а) H H -g" aф-о e о a О о This semester you learned about the Grignard reactions of aldehydes and ketones. Which of the following compounds can not be synthesized by the Grignard reaction of the corresponding aldehyde/ketone with EtMgBr followed by acidic work up. (MULTIPLE ANSWER) OCH (A) (D) OH OH OCH2CH3 OH OD ПС ПВ ОА For the following Grignard reaction, select...
Show how you would synthesize each compound from benzene, toluene, or phenol using the following reactions:...
Show how you would synthesize each compound from benzene, toluene, or phenol using the following reactions: Reactions 1. Halogenation 2. Nitration 3. Sulfonation 4. Friedel-Crafts acylation 5. Friedel-Crafts alkylation 6. Oxidation of methyl group 7. Reduction of nitro group • Choose the starting material from the drop-down list • Enter the number(s) of the desired reactions in the order that you wish to use them without commas between • If a reaction is used more than once, enter its number...
please help in all sections asap!! Which type of electron is the highest in energy? An electron in an an...
please help in all sections asap!!
Which type of electron is the highest in energy? An electron in an anti-bonding molecular orbital. An electron in a bonding molecular orbital. An electron in an atomic orbital. O A non-bonding electron. Choose a systematic name for the following compound. 1,4 dimethyl ethyl benzene 1,4 diethyl methyl benzene 1,4-diisopropylbenzene 1,4 dipropylbenzene Answer the following questions. -OR Would you expect the above compound to be aromatic? Yes No Choose the correct explanations for the...
18. Which of the following compound(s) would undergo mutarotation in aqueous solution? 19. Draw the chair...
18.
Which of the following compound(s) would undergo mutarotation in
aqueous solution?
19. Draw the chair conformation of a-D-galactopyranose.
20. Which of the following compound(s) is a glycoside?
21. Provide the reagents neccesary to carry out the following
conversion.
22. Predict the product(s) for the following reaction.
23. D-glucose & D-galactose are ______epimers of each
other.
24. Predict the product(s) for the following reaction.
25. Which of the following compound(s) would produce D-glucose
and D-mannose when treated with HCN followed...
Can you help me identify reagent (i), Compound 8 and Compound 12 in the reaction scheme?...
Can you help me identify reagent (i), Compound 8 and
Compound 12 in the reaction scheme?
You have laboratory data on all the compounds in the
synthesis, however the amount of data available to you varies. Some
have the entirety of the spectral data, others have as little as
the elemental analysis. Use the laboratory data to help you
discover which reaction has been performed.
The lab data for Compound 8 and 12 is as
follows:
You can use any...
please help in all sections asap! The following two drawings are resonance structures of one compound....
please help in all sections asap!
The following two drawings are resonance structures of one compound. a-o But the following two drawings are not resonance structures Not resonance structures They are, in fact, two different compounds. Choose the correct explanation(s). Select all that apply. Benzene does not have three C-C single bond and three C-C double bonds. In fact, all six C-C bonds of the ring have the same bond order and same length. Benzene have three C- single bond...
please help in all sections asap!! Identify the reagents for each of the following transformations. Select...
please help in all sections asap!!
Identify the reagents for each of the following transformations. Select all that apply. V -a HC=CNa MCPBA NaOEt H2O2, NaOH NBS, heat Conc. H2S04, heat OBH3-THF OH PCC, CH2Cl2 Conc. H2SO4, heat OBH3-THF HC=CNa MCPBA H2O2, NaOH NBS, heat HCCNa ОМСРВА H2O2, NaOH PCC, CH2Cl2 Conc. H2SO4, heat The following two drawings are resonance structures of one compound. But the following two drawings are not resonance structures Not resonance structures They are, in fact,...
D Question 2 2 pts Which reagents would be best used to perform the following transformation?...
D Question 2 2 pts Which reagents would be best used to perform the following transformation? Time Runn 43 Minute OOH 1) 1. H+ ЛОН HO 2. Mgº 3. CO2 4. H30 2) 1. MeMgBr 2. H307 3. H2SO4 3) 1. NaHCO, 2. H30* 4) 1.HHO OH | 5) 1. HCN 2. CrOz/H20 2. CrOy/H20 3. H307 03 5 Predict the major product of the following reaction. & Hochs H" (eat) H3C 3) H3C -CH; 5) HyC-CH3 4) CH3 H3C-N-CH3...
Which compound(s) would be an activator and an op-director? Enter all numbers in numerical order. COCH3 Br Which two starting materials can be used to prepare the compound in the box? Enter two numbers, in numerical order.
Which starting material would give the following ketone product using the Friedel Crafts acylation adidas όόόό Which two starting materials can be used to prepare the compound in the box? Enter two numbers, in numerical order. O Trieu
Practice ACS questions:
Choose the compound which would be insoluble in aq. sodium hydroxide solution. а) H H -g" aф-о e о a О о This semester you learned about the Grignard reactions of aldehydes and ketones. Which of the following compounds can not be synthesized by the Grignard reaction of the corresponding aldehyde/ketone with EtMgBr followed by acidic work up. (MULTIPLE ANSWER) OCH (A) (D) OH OH OCH2CH3 OH OD ПС ПВ ОА For the following Grignard reaction, select...
Show how you would synthesize each compound from benzene, toluene, or phenol using the following reactions: Reactions 1. Halogenation 2. Nitration 3. Sulfonation 4. Friedel-Crafts acylation 5. Friedel-Crafts alkylation 6. Oxidation of methyl group 7. Reduction of nitro group • Choose the starting material from the drop-down list • Enter the number(s) of the desired reactions in the order that you wish to use them without commas between • If a reaction is used more than once, enter its number...
please help in all sections asap!!
Which type of electron is the highest in energy? An electron in an anti-bonding molecular orbital. An electron in a bonding molecular orbital. An electron in an atomic orbital. O A non-bonding electron. Choose a systematic name for the following compound. 1,4 dimethyl ethyl benzene 1,4 diethyl methyl benzene 1,4-diisopropylbenzene 1,4 dipropylbenzene Answer the following questions. -OR Would you expect the above compound to be aromatic? Yes No Choose the correct explanations for the...
18.
Which of the following compound(s) would undergo mutarotation in
aqueous solution?
19. Draw the chair conformation of a-D-galactopyranose.
20. Which of the following compound(s) is a glycoside?
21. Provide the reagents neccesary to carry out the following
conversion.
22. Predict the product(s) for the following reaction.
23. D-glucose & D-galactose are ______epimers of each
other.
24. Predict the product(s) for the following reaction.
25. Which of the following compound(s) would produce D-glucose
and D-mannose when treated with HCN followed...
Can you help me identify reagent (i), Compound 8 and
Compound 12 in the reaction scheme?
You have laboratory data on all the compounds in the
synthesis, however the amount of data available to you varies. Some
have the entirety of the spectral data, others have as little as
the elemental analysis. Use the laboratory data to help you
discover which reaction has been performed.
The lab data for Compound 8 and 12 is as
follows:
You can use any...
please help in all sections asap!
The following two drawings are resonance structures of one compound. a-o But the following two drawings are not resonance structures Not resonance structures They are, in fact, two different compounds. Choose the correct explanation(s). Select all that apply. Benzene does not have three C-C single bond and three C-C double bonds. In fact, all six C-C bonds of the ring have the same bond order and same length. Benzene have three C- single bond...
please help in all sections asap!!
Identify the reagents for each of the following transformations. Select all that apply. V -a HC=CNa MCPBA NaOEt H2O2, NaOH NBS, heat Conc. H2S04, heat OBH3-THF OH PCC, CH2Cl2 Conc. H2SO4, heat OBH3-THF HC=CNa MCPBA H2O2, NaOH NBS, heat HCCNa ОМСРВА H2O2, NaOH PCC, CH2Cl2 Conc. H2SO4, heat The following two drawings are resonance structures of one compound. But the following two drawings are not resonance structures Not resonance structures They are, in fact,...
D Question 2 2 pts Which reagents would be best used to perform the following transformation? Time Runn 43 Minute OOH 1) 1. H+ ЛОН HO 2. Mgº 3. CO2 4. H30 2) 1. MeMgBr 2. H307 3. H2SO4 3) 1. NaHCO, 2. H30* 4) 1.HHO OH | 5) 1. HCN 2. CrOz/H20 2. CrOy/H20 3. H307 03 5 Predict the major product of the following reaction. & Hochs H" (eat) H3C 3) H3C -CH; 5) HyC-CH3 4) CH3 H3C-N-CH3...
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