Homework Answers
The reaction is an oxidation reaction.
where primary alcohol has been oxidized to carboxylic acid.
so we need an oxidizing agent .
the suitable reagent for this reaction is CrO3. H+
so answer is B
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Which could be used in the following conversion? CH2OH CO2H A. LiAlH4 B. CrO3, H+ C....
Which reagent is required in the box for Reaction 1? A) CrO3, HCl, Pyridine B) LDA C) HBr D) NaOH E) TsCl w/ pyridine F...
Which reagent is required in the box for Reaction
1?
A) CrO3, HCl, Pyridine
B) LDA
C) HBr
D) NaOH
E) TsCl w/ pyridine
F) PBr3
G) LiAlH4
Consider the structures of Intermediate Product Y and the final
product. What would be the best reagent to place in the box for
Reaction 2?
A) H2O
B) NaOH
C) Mg
D) (CH3)3COK
E) NaBH4
F) HCl
G) CH3Br
E) CrO3, H2SO4, H2O
11 Reaction 1 Intermediate Product Y Reaction 2 HO
Which compound could be subjected to a haloform reaction to produce m-chlorobenzoic acid? O CH2OH CO2H...
Which compound could be subjected to a haloform reaction to produce m-chlorobenzoic acid? O CH2OH CO2H CCH2CH3 CCH3 CI CI CI I II III IV Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer.
Which acid group would most easily undergo decarboxylation? e. HOC d. CO2H HOQC CO2H a. C....
Which acid group would most easily undergo decarboxylation? e. HOC d. CO2H HOQC CO2H a. C. CO2H b. a. Ob O c. O d. Oe.
+ lidt 6) How would you perform the following transformation? OCH CHE A) NaBH4 B) LiAlH4 C) 1. DIBAL-H 2. H20 D)...
+ lidt 6) How would you perform the following transformation? OCH CHE A) NaBH4 B) LiAlH4 C) 1. DIBAL-H 2. H20 D) 1. SOCI2 2. LiAlH(O-1-Bu)3 7) What reagent can be used to convert 2-methylbutan-1-ol into 2-methylbutanal? A) LiAlH4 B) Na2Cr207 C) 03 D) KMnO4 E) PCC 9) Show how you would perform the following synthesis. A) 1. 03 2. (CH3)2S B) KMnO4, cold, basic C) Os04 D) 1. mCPBA 2. potassium dichromate 25) Provide a detailed, stepwise mechanism for...
Choose the best reagent(s) for carrying out the following conversion from the list provided below. a....
Choose the best reagent(s) for carrying out the following conversion from the list provided below. a. 1. e. f. g. CH3MgBr, ether H307 PBr3 NaOH (CH3)3SiC1, (CH3CH2)3N CH3MgBr, ether H30+ LiAlH4, ether 1. p-TosC1, pyridine 2. NaOH CrO3, H2SO4, H2O 1. NaBH4, ethanol 2. H30 Dess-Martin periodinane , CH2Cl2 1. h. 3. d. 1. H30+ HO CH: OH
What metabolic pathway forms the following conversion OH I-O C=0 C=0 H-C-OH C=0 HO-C-H 2 4...
What metabolic pathway forms the following conversion OH I-O C=0 C=0 H-C-OH C=0 HO-C-H 2 4 H-CH H-C-OH H-C-OH H 1 CH2OH (A) Glycolysis (B) Kreb's Cycle (C) Chemiosmosis (D) Fermentation a.(a) Ob.(b) OC(C) d.(d) Moving to another question will save this response
PROBLEM 7 13 Assign E or Z configuration to the following alkenes: (a) H3C CH2OH (b)...
PROBLEM 7 13 Assign E or Z configuration to the following alkenes: (a) H3C CH2OH (b) C CH2CH3 CH3CH2 C снзо сњењенз (c) CH3 (d) H CN CO2H с с H3C CH2NH2 CH2OH PROBLEM 7-14 Assign stereochemistry (E or Z) to the double bond in the following com pound, and convert the drawing into a skeletal structure (red O);
1. Which of the following molecules has the lowest strain energy? a. Cyclobutane b. Cyclohexane c. Cycloheptane d....
1. Which of the following molecules has the lowest strain energy? a. Cyclobutane b. Cyclohexane c. Cycloheptane d. Cyclopropane 2. Which of the following arranges the groups in order of decreasing priority according to the sequence rules? a. CH3 > CH2CH3 > CH2OH > CO2H c. CH2OH > CO2H > CH2CH3 > CH3 b. CH3 > CH2CH3 > CO2H >CH2OH d. CO2H > CH2OH > CH2CH3 > CH3 3. Which of the following structures represent a meso compound? a. b....
QUESTION 18: Which of the following compounds gives a 1M aqueous solution having the highest pH?...
QUESTION 18: Which of the following compounds gives a 1M aqueous solution having the highest pH? A. (CH3)4N+OH– B. (CH3)4N+Cl– C. (CH3)3N D. (CH3)3NH+Cl– QUESTION 19: The overall conversion RBr →→ RCH2NH2 can be accomplished by successive application of which of these sets of reagents? A. Mg, ether; then NH3 B. NaN3; then LiAlH4 C. NaCN; then LiAlH4 D. H2C=O; then NH3 E. H2NOH; then LiAlH4 QUESTION 20: Which sequence is suitable for preparing butylamine from 1-propanol? A. KMnO4, then...
Specify the reagent you would use in each step of the following synthesis: Specify the reagent...
Specify the reagent you would use in each step of the following
synthesis:
Specify the reagent you would use in each step of the following synthesis: step 1 step 1, step 2 step 2 =cHCH3 Reagents Available a. LiAlH4 b. H2SO4 c. HCI f. PBr3 k. CH3CH MgBr g. Dess-Martin periodinane (DMP) I. CHgMgBr (phenylmagnesium bromide) h. NaH m. (CH3)2CHMgBr i, NaOH n. Cro3 j. CH3MgBr d. HBO e. SOCI2 Write the letters of the reagents in the boxes below....
Which reagent is required in the box for Reaction
1?
A) CrO3, HCl, Pyridine
B) LDA
C) HBr
D) NaOH
E) TsCl w/ pyridine
F) PBr3
G) LiAlH4
Consider the structures of Intermediate Product Y and the final
product. What would be the best reagent to place in the box for
Reaction 2?
A) H2O
B) NaOH
C) Mg
D) (CH3)3COK
E) NaBH4
F) HCl
G) CH3Br
E) CrO3, H2SO4, H2O
11 Reaction 1 Intermediate Product Y Reaction 2 HO
Which compound could be subjected to a haloform reaction to produce m-chlorobenzoic acid? O CH2OH CO2H CCH2CH3 CCH3 CI CI CI I II III IV Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer.
Which acid group would most easily undergo decarboxylation? e. HOC d. CO2H HOQC CO2H a. C. CO2H b. a. Ob O c. O d. Oe.
+ lidt 6) How would you perform the following transformation? OCH CHE A) NaBH4 B) LiAlH4 C) 1. DIBAL-H 2. H20 D) 1. SOCI2 2. LiAlH(O-1-Bu)3 7) What reagent can be used to convert 2-methylbutan-1-ol into 2-methylbutanal? A) LiAlH4 B) Na2Cr207 C) 03 D) KMnO4 E) PCC 9) Show how you would perform the following synthesis. A) 1. 03 2. (CH3)2S B) KMnO4, cold, basic C) Os04 D) 1. mCPBA 2. potassium dichromate 25) Provide a detailed, stepwise mechanism for...
Choose the best reagent(s) for carrying out the following conversion from the list provided below. a. 1. e. f. g. CH3MgBr, ether H307 PBr3 NaOH (CH3)3SiC1, (CH3CH2)3N CH3MgBr, ether H30+ LiAlH4, ether 1. p-TosC1, pyridine 2. NaOH CrO3, H2SO4, H2O 1. NaBH4, ethanol 2. H30 Dess-Martin periodinane , CH2Cl2 1. h. 3. d. 1. H30+ HO CH: OH
What metabolic pathway forms the following conversion OH I-O C=0 C=0 H-C-OH C=0 HO-C-H 2 4 H-CH H-C-OH H-C-OH H 1 CH2OH (A) Glycolysis (B) Kreb's Cycle (C) Chemiosmosis (D) Fermentation a.(a) Ob.(b) OC(C) d.(d) Moving to another question will save this response
PROBLEM 7 13 Assign E or Z configuration to the following alkenes: (a) H3C CH2OH (b) C CH2CH3 CH3CH2 C снзо сњењенз (c) CH3 (d) H CN CO2H с с H3C CH2NH2 CH2OH PROBLEM 7-14 Assign stereochemistry (E or Z) to the double bond in the following com pound, and convert the drawing into a skeletal structure (red O);
1. Which of the following molecules has the lowest strain energy? a. Cyclobutane b. Cyclohexane c. Cycloheptane d. Cyclopropane 2. Which of the following arranges the groups in order of decreasing priority according to the sequence rules? a. CH3 > CH2CH3 > CH2OH > CO2H c. CH2OH > CO2H > CH2CH3 > CH3 b. CH3 > CH2CH3 > CO2H >CH2OH d. CO2H > CH2OH > CH2CH3 > CH3 3. Which of the following structures represent a meso compound? a. b....
Specify the reagent you would use in each step of the following
synthesis:
Specify the reagent you would use in each step of the following synthesis: step 1 step 1, step 2 step 2 =cHCH3 Reagents Available a. LiAlH4 b. H2SO4 c. HCI f. PBr3 k. CH3CH MgBr g. Dess-Martin periodinane (DMP) I. CHgMgBr (phenylmagnesium bromide) h. NaH m. (CH3)2CHMgBr i, NaOH n. Cro3 j. CH3MgBr d. HBO e. SOCI2 Write the letters of the reagents in the boxes below....
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