why is the answer D and not A? can someone draw this out and
explain for me? i thought the K2CrO7 would not affect the Br? thank
you so much!Homework Answers
Option (d) is correct.
In option A. First benzene reacts with CH3Cl/AlCl3. So toluene(means CH3 attached to benzene) formed. But after Br2/FeBr3 it attached to CH3 not benzene. That's why first we have to oxidized it into COOH group. And As COOH is meta directing so Br attached at meta position
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why is the answer D and not A? can someone draw this out and
explain for...
provide the reagents necessary to carry out the following conversion. Testbank, Question 095 Provide the reagents...
provide the reagents necessary to carry out the following
conversion.
Testbank, Question 095 Provide the reagents necessary to carry out the following conversion. OOH NH2 Br Br Choose the correct reagents for step 1. xs Br2 / FeBr3 NaNO2/ HCI / < 5°C OH3PO2 KMnO4/ NaOH / H20 CH3CI / AICI: Huden/shared/assignment/test/aalistiuni?idmasnmt2593399 #N10170 Choose the correct reagents for step 2. NaNO2 / HCI / < 5°C xs Br2 / FeBr3 H3PO2 O KMnO4 / NaOH / H2O CH3CI / AICI:...
Which set of reagents will accomplish the following transformation? COOH NH Br A) B) C) 1)...
Which set of reagents will accomplish the following transformation? COOH NH Br A) B) C) 1) CH;CI / AICI 2) Br2/FeBrz 3) Conc. KMnO4 OH, A. then H30 4) Cl2/AICI; 5) HNO3 H2SO4 6) Sn/HCI 1) CH3C1 / AICI 2) Conc KMnO4 OH, A, then H30* 3) HNO; / H2SO4 4) Sn HCI 5) Bry/FeBrz 6) C12/AICI: 1) CH,CI/AICI: 2) Bry/FeBrz 3) Cly/AICI: 4) Conc. KMnO OH, Athen H30 5) HNO3 /H SO. 6) Sn/HCI B) D) 1) HNO; H2SO4...
please help in all sections asap!! Provide the reagents necessary to carry out the following conversion....
please help in all sections asap!!
Provide the reagents necessary to carry out the following conversion. ОСН Br Br NO2 Choose the correct reagents for step 1 fuming H2SO4 HNO3/H2S04 excess Br2/ FeBr3 dilute H2SO4 O Cl2/FeCly O CH3ONA Choose the correct reagents for step 2. Cl2/ FeCl3 HNO3/H2SO4 CH3ONA fuming H2SO4 excess Br2/ FeBr3 dilute H2SO4 Choose the correct reagents for step 3 CH3ONA HNO3/ H2SO4 O excess Br2/ FeBr3 Odilute H2S04 fuming H2SO C2/ FeCl Choose the correct...
please help in all sections!! Provide the reagents necessary to carry out the following conversion. Choose...
please help in all sections!!
Provide the reagents necessary to carry out the following conversion. Choose the correct reagents for step 1. AICI AICI CI CH3CI/ AICI3 CH3CI/ FeCl Choose the correct reagents for step 2 Zn(Hg), HCI A Zn(Hg), H2SO Zn, HCI A Mg(Hg), HCI A Predict the major product for the following reaction. B Feble 11 11 IV V E2 > Identify the electrophile in the bromination of benzene. Br Br2 Br-Br-Fe-Br Br FeBr2 FeBr3 Br 11 11...
PLEASE ANSWER ALL QUESTIONS 41) Provide the major organic product of the following reaction. Bry, FeBry...
PLEASE ANSWER ALL QUESTIONS
41) Provide the major organic product of the following reaction. Bry, FeBry 42) Provide the major organic product that results when benzene is treated with the following sequence of reagents: 1. HNO3, H2SO4 2. Br2, FeBr3. Answer: NO2 43) Explain why Friedel-Crafts alkylation reactions are prone to poly alkylation, whereas Friedel- Crafts acylation reactions are not prone to polyacylation? 44) Which series of reagents would be required to perform the following synthesis? A) 1. CICH2CH2CH3, AICI;...
Select the reagents you would use to synthesize the compound below from benzene. (More than one...
Select the reagents you would use to synthesize the compound
below from benzene.
(More than one step is required. If no third step is needed,
choose (none).)
Reagents Available f. KMnO4, H20 g. H2, Pd/C h. SO3, H2SO4 i. NaOH, H2O a. Br2, FeBr3 b. Cl2, FeCl 0 d. CH3CI, AICl3 Br e. CH3COCI, AICl3 N-bromosuccinimide (NBS) ball & stick labels Step 1: Step 2 Step 3
36. Which of the following compounds is able to undergo a self-aldol condensation? A. phenylethanal B....
36. Which of the following compounds is able to undergo a self-aldol condensation? A. phenylethanal B. formaldehyde C. benzaldehyde D. 2,2-dimethylpropanal 37. The best synthesis of 1,4-dimethyl-2-nitrobenzene is: A. Benzene 1. HNO3, H2SO4 2. 2 CH,CI, 2 AICI: 1. HNO3, H2SO4 2. CH3CI, AICI: HNO3, H2SO4 B. toluene C. p-xylene D.m-nitrotoluene CH3CI, AICI: 38. Which of these is the most reliable way to make 3-heptene? A. CH,CH,CHBECH,CH,CH,CH3 + NaOCH3, heat B. CH3CH2CH-0 + Ph3P-CHCH,CH.CH C. CH CH CHOHCH2CH2CH2CH3 + H2SO4,...
please write the steps needed to get this product. A NaBH4/H:0 S KMnO4 HNO3 H2SO4 K...
please write the steps needed to get this product.
A NaBH4/H:0 S KMnO4 HNO3 H2SO4 K HNO3 H2SO4 B LiAlH4/H:07 T CH3MgBr/H:0* U 1. LDA/ 2. CH Br C Dess-Martin L Nal D CrOz/H:07 M H3PO4 V NaCN E H/Pd N Bry/FeBr3 W NH 0 CH:COCI/AICI: X CH3NH2 P CH:CH-CT/AICI: Y SOCI: F SnCl/H30* 1. Hg(OAc)2, H2O/THF G 2. NaBHA HH2SO4, H2O, HgSO4 1. BH3, THF 2. H2O2, OH Q H3O+/H20 Z CH OH R KOH O CHICHI CH3CH CH:CH-C-OH...
D Below is a list of reagents that will be used for the following question (reactions...
D Below is a list of reagents that will be used for the following question (reactions 1-6). A. 1, KCN 2. H, H2O, A B. 1. NaNO,, HCI 2. CuCN c. 1. Mg 2. CO2 3. H2O D. 1. NaH 2. Br E. 1. Mg 2. ro 3. H, H20 F. PCC G. KMnO4 H2O, HO J. 1. Mg 2. K. AICI H. 1. Mg 2. Lo 3. H30* 4. PCC O 3. H, H2O 4. PCC Determine the reagents...
How would you convert an unsaturated fatty acid into a saturated fatty acid A. KMnO4, "OH,...
How would you convert an unsaturated fatty acid into a saturated fatty acid A. KMnO4, "OH, heat B. "OH,H,O, heat; then H,0 C. Hz, Ni, pressure D. H,0,H,O, heat 26. What structure has the following proton NMR spectrum? 'H NMR: doublet, 6.6 ppm, 2H doublet, 7.8 ppm, 2H broad singlet, 4.2 ppm, 2H singlet, 2.1 ppm, 3H HUN 27. Which of the following is the correct synthesis of the compound shown? CH, Br o Na Na o CH,Br B. T...
provide the reagents necessary to carry out the following
conversion.
Testbank, Question 095 Provide the reagents necessary to carry out the following conversion. OOH NH2 Br Br Choose the correct reagents for step 1. xs Br2 / FeBr3 NaNO2/ HCI / < 5°C OH3PO2 KMnO4/ NaOH / H20 CH3CI / AICI: Huden/shared/assignment/test/aalistiuni?idmasnmt2593399 #N10170 Choose the correct reagents for step 2. NaNO2 / HCI / < 5°C xs Br2 / FeBr3 H3PO2 O KMnO4 / NaOH / H2O CH3CI / AICI:...
Which set of reagents will accomplish the following transformation? COOH NH Br A) B) C) 1) CH;CI / AICI 2) Br2/FeBrz 3) Conc. KMnO4 OH, A. then H30 4) Cl2/AICI; 5) HNO3 H2SO4 6) Sn/HCI 1) CH3C1 / AICI 2) Conc KMnO4 OH, A, then H30* 3) HNO; / H2SO4 4) Sn HCI 5) Bry/FeBrz 6) C12/AICI: 1) CH,CI/AICI: 2) Bry/FeBrz 3) Cly/AICI: 4) Conc. KMnO OH, Athen H30 5) HNO3 /H SO. 6) Sn/HCI B) D) 1) HNO; H2SO4...
please help in all sections asap!!
Provide the reagents necessary to carry out the following conversion. ОСН Br Br NO2 Choose the correct reagents for step 1 fuming H2SO4 HNO3/H2S04 excess Br2/ FeBr3 dilute H2SO4 O Cl2/FeCly O CH3ONA Choose the correct reagents for step 2. Cl2/ FeCl3 HNO3/H2SO4 CH3ONA fuming H2SO4 excess Br2/ FeBr3 dilute H2SO4 Choose the correct reagents for step 3 CH3ONA HNO3/ H2SO4 O excess Br2/ FeBr3 Odilute H2S04 fuming H2SO C2/ FeCl Choose the correct...
please help in all sections!!
Provide the reagents necessary to carry out the following conversion. Choose the correct reagents for step 1. AICI AICI CI CH3CI/ AICI3 CH3CI/ FeCl Choose the correct reagents for step 2 Zn(Hg), HCI A Zn(Hg), H2SO Zn, HCI A Mg(Hg), HCI A Predict the major product for the following reaction. B Feble 11 11 IV V E2 > Identify the electrophile in the bromination of benzene. Br Br2 Br-Br-Fe-Br Br FeBr2 FeBr3 Br 11 11...
PLEASE ANSWER ALL QUESTIONS
41) Provide the major organic product of the following reaction. Bry, FeBry 42) Provide the major organic product that results when benzene is treated with the following sequence of reagents: 1. HNO3, H2SO4 2. Br2, FeBr3. Answer: NO2 43) Explain why Friedel-Crafts alkylation reactions are prone to poly alkylation, whereas Friedel- Crafts acylation reactions are not prone to polyacylation? 44) Which series of reagents would be required to perform the following synthesis? A) 1. CICH2CH2CH3, AICI;...
Select the reagents you would use to synthesize the compound
below from benzene.
(More than one step is required. If no third step is needed,
choose (none).)
Reagents Available f. KMnO4, H20 g. H2, Pd/C h. SO3, H2SO4 i. NaOH, H2O a. Br2, FeBr3 b. Cl2, FeCl 0 d. CH3CI, AICl3 Br e. CH3COCI, AICl3 N-bromosuccinimide (NBS) ball & stick labels Step 1: Step 2 Step 3
36. Which of the following compounds is able to undergo a self-aldol condensation? A. phenylethanal B. formaldehyde C. benzaldehyde D. 2,2-dimethylpropanal 37. The best synthesis of 1,4-dimethyl-2-nitrobenzene is: A. Benzene 1. HNO3, H2SO4 2. 2 CH,CI, 2 AICI: 1. HNO3, H2SO4 2. CH3CI, AICI: HNO3, H2SO4 B. toluene C. p-xylene D.m-nitrotoluene CH3CI, AICI: 38. Which of these is the most reliable way to make 3-heptene? A. CH,CH,CHBECH,CH,CH,CH3 + NaOCH3, heat B. CH3CH2CH-0 + Ph3P-CHCH,CH.CH C. CH CH CHOHCH2CH2CH2CH3 + H2SO4,...
please write the steps needed to get this product.
A NaBH4/H:0 S KMnO4 HNO3 H2SO4 K HNO3 H2SO4 B LiAlH4/H:07 T CH3MgBr/H:0* U 1. LDA/ 2. CH Br C Dess-Martin L Nal D CrOz/H:07 M H3PO4 V NaCN E H/Pd N Bry/FeBr3 W NH 0 CH:COCI/AICI: X CH3NH2 P CH:CH-CT/AICI: Y SOCI: F SnCl/H30* 1. Hg(OAc)2, H2O/THF G 2. NaBHA HH2SO4, H2O, HgSO4 1. BH3, THF 2. H2O2, OH Q H3O+/H20 Z CH OH R KOH O CHICHI CH3CH CH:CH-C-OH...
D Below is a list of reagents that will be used for the following question (reactions 1-6). A. 1, KCN 2. H, H2O, A B. 1. NaNO,, HCI 2. CuCN c. 1. Mg 2. CO2 3. H2O D. 1. NaH 2. Br E. 1. Mg 2. ro 3. H, H20 F. PCC G. KMnO4 H2O, HO J. 1. Mg 2. K. AICI H. 1. Mg 2. Lo 3. H30* 4. PCC O 3. H, H2O 4. PCC Determine the reagents...
How would you convert an unsaturated fatty acid into a saturated fatty acid A. KMnO4, "OH, heat B. "OH,H,O, heat; then H,0 C. Hz, Ni, pressure D. H,0,H,O, heat 26. What structure has the following proton NMR spectrum? 'H NMR: doublet, 6.6 ppm, 2H doublet, 7.8 ppm, 2H broad singlet, 4.2 ppm, 2H singlet, 2.1 ppm, 3H HUN 27. Which of the following is the correct synthesis of the compound shown? CH, Br o Na Na o CH,Br B. T...
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