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Organic chem problem, need help
Which combination of starting materials will produce compound 1? Ph. I...
Organic II help Which combination of starting materials will produce compound 1? HO MgBr "MgBr MgBr...
Organic II help
Which combination of starting materials will produce compound 1? HO MgBr "MgBr MgBr B C D 1) A/E and B/F 2) B/D and C/F 3) A/F and C/D 4) B/F and C/E 5) A/D and B/E 3 0 1 2 04
Not sure about this one Which combination of starting materials will produce compound Old room 1)...
Not sure about this one
Which combination of starting materials will produce compound Old room 1) A/E and B/D 2) B/E and C/D 3) A/D and C/E 4) B/D and C/E 5) A/E and C/D
organic chem, i like your answer immediately 3. A compound with molecular formula of C4H8O2 has...
organic chem, i like your answer immediately
3. A compound with molecular formula of C4H8O2 has one singlet H-NMR peak at 8 3.7 ppm. This compound has a strong IR absorption at 1122 cm!. There is no carbonyl group in this compound. What is the structure of this compound? A. B. C D. 3 1
#6 Which combination(s) of organic bromide and carbonyl compound can be used to prepare the alcohol...
#6 Which combination(s) of organic bromide and carbonyl compound can be used to prepare the alcohol in the box by reaction of the Grignard reagent derived from the alkyl bromide with the carbonyl compound? Wrong Answer B OCH CH3Br CH3Br 3 a) only 1 b) only 1 and 2 c) 1, 2 and 3 d) only 3 and 4 e) 1,2,and 4
Help please Compound 1 could be made from the acid catalyzed reaction of which two starting...
Help please
Compound 1 could be made from the acid catalyzed reaction of which two starting materials? my HOOH HOM OH 1) A and C 2) A and D 3) B and C 4) B and D 5) no combination will work
#6 Which combination(s) of organic bromide and carbonyl compound can be used to prepare the alcohol...
#6 Which combination(s) of organic bromide and carbonyl compound can be used to prepare the alcohol in the box by reaction of the Grignard reagent derived from the alkyl bromide with the carbonyl compound? Wrong Answer B OCH OCH CH3Br CH3BT OH a) only 1 b) only 1 and 2 c) 1, 2 and 3 d) only 3 and 4 e) 1,2,and 4
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...
Hello I need some help with these organic chem pre lab questions for the extraction of...
Hello
I need some help with these organic chem pre lab questions for
the extraction of trimyristin from nutmeg
4.(1) What technique is used to ensure as much as possible trimyristin is extracted from the nutmeg? 5. (6 pts.) Indicate whether the following statements are true (T) or false (F) AND correct any of the false statements. a. The functional group present in trimyristin is a carboxylic acid group b. Pure trimyristin is a liquid at room temperature. c. The...
extra credit orgo chem NaBH MOH 1.Write two starting materials (five or fewer C's) that react...
extra credit orgo chem
NaBH MOH 1.Write two starting materials (five or fewer C's) that react to form the target molecule starting from any carbonyl compound and any organometallic reagent. OH Part IV. Mechanistic Puzzlers (16 pts) 10. Reduction of cyclohexanone using lithium aluminum hydride gives a deuterated alcohol when D.O is used instead of H.O in the workup step. Account for this outcome with a mechanism, showing curved arrows, the key intermediate, and lone pairs and charges. (6 pts)...
6.24 With methyl, ethyl, or cyclopentyl halides as your organic starting materials and using any needed...
6.24 With methyl, ethyl, or cyclopentyl halides as your organic starting materials and using any needed solvents or inorganic reagents, outline syntheses of each of the following. More than one step may be necessary and you need not repeat steps carried out in earlier parts of this problem (a) CH3 (e) CH3SH (i) CH30CH3 (b) (f) (j) SH OMe (c) CH3OH (g) CH3CN (d) (h) CN ОН
Organic II help
Which combination of starting materials will produce compound 1? HO MgBr "MgBr MgBr B C D 1) A/E and B/F 2) B/D and C/F 3) A/F and C/D 4) B/F and C/E 5) A/D and B/E 3 0 1 2 04
Not sure about this one
Which combination of starting materials will produce compound Old room 1) A/E and B/D 2) B/E and C/D 3) A/D and C/E 4) B/D and C/E 5) A/E and C/D
organic chem, i like your answer immediately
3. A compound with molecular formula of C4H8O2 has one singlet H-NMR peak at 8 3.7 ppm. This compound has a strong IR absorption at 1122 cm!. There is no carbonyl group in this compound. What is the structure of this compound? A. B. C D. 3 1
#6 Which combination(s) of organic bromide and carbonyl compound can be used to prepare the alcohol in the box by reaction of the Grignard reagent derived from the alkyl bromide with the carbonyl compound? Wrong Answer B OCH CH3Br CH3Br 3 a) only 1 b) only 1 and 2 c) 1, 2 and 3 d) only 3 and 4 e) 1,2,and 4
Help please
Compound 1 could be made from the acid catalyzed reaction of which two starting materials? my HOOH HOM OH 1) A and C 2) A and D 3) B and C 4) B and D 5) no combination will work
#6 Which combination(s) of organic bromide and carbonyl compound can be used to prepare the alcohol in the box by reaction of the Grignard reagent derived from the alkyl bromide with the carbonyl compound? Wrong Answer B OCH OCH CH3Br CH3BT OH a) only 1 b) only 1 and 2 c) 1, 2 and 3 d) only 3 and 4 e) 1,2,and 4
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...
Hello
I need some help with these organic chem pre lab questions for
the extraction of trimyristin from nutmeg
4.(1) What technique is used to ensure as much as possible trimyristin is extracted from the nutmeg? 5. (6 pts.) Indicate whether the following statements are true (T) or false (F) AND correct any of the false statements. a. The functional group present in trimyristin is a carboxylic acid group b. Pure trimyristin is a liquid at room temperature. c. The...
extra credit orgo chem
NaBH MOH 1.Write two starting materials (five or fewer C's) that react to form the target molecule starting from any carbonyl compound and any organometallic reagent. OH Part IV. Mechanistic Puzzlers (16 pts) 10. Reduction of cyclohexanone using lithium aluminum hydride gives a deuterated alcohol when D.O is used instead of H.O in the workup step. Account for this outcome with a mechanism, showing curved arrows, the key intermediate, and lone pairs and charges. (6 pts)...
6.24 With methyl, ethyl, or cyclopentyl halides as your organic starting materials and using any needed solvents or inorganic reagents, outline syntheses of each of the following. More than one step may be necessary and you need not repeat steps carried out in earlier parts of this problem (a) CH3 (e) CH3SH (i) CH30CH3 (b) (f) (j) SH OMe (c) CH3OH (g) CH3CN (d) (h) CN ОН
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