please help with these 2 questions
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please help with these 2 questions
the following is formed in the step shown below? CH3CH2...
Draw a structural formula for the major product of the reaction shown. CH3CH2 S=CHCH2 The CH3CH2...
Draw a structural formula for the major product of the reaction shown. CH3CH2 S=CHCH2 The CH3CH2 Draw a structural formula for the major product of the reaction shown. CH3 CH3CHCH=CH2 Draw a structural formula for the major product of the reaction shown. Cl2 CH3CH2CH2CH=CH2 - H2O Draw structural formulas for all alkenes that could be used to prepare the alcohol shown below by oxymercuration. H3COH , 1. Hg(OAc)2, H2O 2. NaBH4 Draw the structure of the major organic product of...
Please help with both questions below. Thank You!! Part A The solution formed upon adding 50.00...
Please help with both questions below. Thank You!!
Part A The solution formed upon adding 50.00 mL of 0.35 M NH4CI to 50.00 mL of 0.35 M NH3 will have a pH that is the pH of the original NH3 solution. t -- Submit My Answers Give Up Provide Feedback Continue
Predict the Products. Can you please show it step by step. It will help me understand...
Predict the Products. Can you please show it step by step. It
will help me understand more. Thank you in advance
2. D2 CH3CH2-C=C-CH3 Indy 3 Lindlar catalyst -C=C-H 1.BH, THF 2.H20, NaOH, H2O KMnO4 H20+ 5. CH3CH2C=CH HgSO4, H2SO4 Н20
For the mechanism step shown below, answer the following questions. A) Identify the reactants, labeled as...
For the mechanism step shown below, answer the following questions. A) Identify the reactants, labeled as A and B underneath each structure, as electrophile and nucleophile. B) Explain what is wrong with the mechanism as shown. C) What is the next step of the mechanism? OH H. CH -C ho - - CH₂ H₂C CH H₃C o CH₂ HC–CH,
please help 13. Consider the carbocations that could be formed from the compounds below through substitution reactio...
please help
13. Consider the carbocations that could be formed from the compounds below through substitution reactions and assuming no rearrangements. Circle the compounds whose carbocations would be stabilized by resonance. Он OH Br OH Br CI OTs Br- Hас. OTf NH2 OMs - CH3
please help in all sections asap!! Provide the reagents necessary to carry out the following conversion. CC...
please help in all sections asap!!
Provide the reagents necessary to carry out the following conversion. CCH3 Choose the correct reagents for step 1. CH3CH2Cl / AICI Cl2 / AICI Bry/ FeBry CH3CCI / AICI: Choose the correct reagents for step 2. NON CH3CH2C / AICI Cl2 / AICI Bry/FeBry o CH,CCI/ AICI Predict the major product for the following reaction. CI/AICI: ОН ОН ОН 0 none of these Provide the reagents necessary to carry out the following conversion. Choose...
Question 3 (continued) (6) The drug phenaglycodol can be synthesized via a 3-step synthesis shown in...
Question 3 (continued) (6) The drug phenaglycodol can be synthesized via a 3-step synthesis shown in Scheme 1 below. Study the synthesis and answer the following questions. HO OEt NaCNag) H2O* in EtOH A Step 1 Step 2 CI CI Compound 3 2 mol B Step 3 followed by H30* HO OH CI phenaglycodol Scheme 1 (1) Identify the electrophile and nucleophile present in Step 1 (2 marks) (1) Draw the structure of Compound A (2 marks) (111) Identify reagent...
please do answer all the questions below. thank you For each of the following complexes, draw...
please do answer all the questions below. thank you
For each of the following complexes, draw the molecular structure and determine the effective atomic numbers. (i) Na[Fe(CN)s(NH3)3l (i) [Cr(H2O)2(NH3)2(en)]Cl (ii) [Co(o-phen)2(NHs)(NCS))CI (iv) (n3-C3Hs)Co(CO)2] (v) [Fe(diphos)(CO)sl in which diphos Ph2PCH2CH2PPh2 and Ph CsHs (10 marks) (i)/ The K for Fe(OH)4]2-is found to be higher than that found in (5 marks) Zn(OH)4]2-and [Cr(OHM. Explain . Cho and coworkers used the following ligand to react with cobalt. Predict how this ligand would bind...
please help in all questions!! Which of the molecules below is the expected major product of...
please help in all questions!!
Which of the molecules below is the expected major product of the following reduction? Na, NH3) Н H Н нн H H For the given compounds answer the following. Compound A Compound B Compound C Identify which compound is expected to be most acidic. Compound A Compound B Compound C Choose the correct option to justify your choice. ODeprotonation of the compound generates an antiaromatic lon. Deprotonation of the compound generates an aromatic ion. Deprotonation...
Mechanisms. (2) For each experimental result shown below, propose a step-by-step "electron-pushing" mechanism, using "curly arrows"....
Mechanisms. (2) For each experimental result shown below, propose a step-by-step "electron-pushing" mechanism, using "curly arrows". Show all intermediates (if there are any) explicitly. (a) HCI CI (b) н" +CH OH OCH, OH
Draw a structural formula for the major product of the reaction shown. CH3CH2 S=CHCH2 The CH3CH2 Draw a structural formula for the major product of the reaction shown. CH3 CH3CHCH=CH2 Draw a structural formula for the major product of the reaction shown. Cl2 CH3CH2CH2CH=CH2 - H2O Draw structural formulas for all alkenes that could be used to prepare the alcohol shown below by oxymercuration. H3COH , 1. Hg(OAc)2, H2O 2. NaBH4 Draw the structure of the major organic product of...
Please help with both questions below. Thank You!!
Part A The solution formed upon adding 50.00 mL of 0.35 M NH4CI to 50.00 mL of 0.35 M NH3 will have a pH that is the pH of the original NH3 solution. t -- Submit My Answers Give Up Provide Feedback Continue
Predict the Products. Can you please show it step by step. It
will help me understand more. Thank you in advance
2. D2 CH3CH2-C=C-CH3 Indy 3 Lindlar catalyst -C=C-H 1.BH, THF 2.H20, NaOH, H2O KMnO4 H20+ 5. CH3CH2C=CH HgSO4, H2SO4 Н20
For the mechanism step shown below, answer the following questions. A) Identify the reactants, labeled as A and B underneath each structure, as electrophile and nucleophile. B) Explain what is wrong with the mechanism as shown. C) What is the next step of the mechanism? OH H. CH -C ho - - CH₂ H₂C CH H₃C o CH₂ HC–CH,
please help
13. Consider the carbocations that could be formed from the compounds below through substitution reactions and assuming no rearrangements. Circle the compounds whose carbocations would be stabilized by resonance. Он OH Br OH Br CI OTs Br- Hас. OTf NH2 OMs - CH3
please help in all sections asap!!
Provide the reagents necessary to carry out the following conversion. CCH3 Choose the correct reagents for step 1. CH3CH2Cl / AICI Cl2 / AICI Bry/ FeBry CH3CCI / AICI: Choose the correct reagents for step 2. NON CH3CH2C / AICI Cl2 / AICI Bry/FeBry o CH,CCI/ AICI Predict the major product for the following reaction. CI/AICI: ОН ОН ОН 0 none of these Provide the reagents necessary to carry out the following conversion. Choose...
Question 3 (continued) (6) The drug phenaglycodol can be synthesized via a 3-step synthesis shown in Scheme 1 below. Study the synthesis and answer the following questions. HO OEt NaCNag) H2O* in EtOH A Step 1 Step 2 CI CI Compound 3 2 mol B Step 3 followed by H30* HO OH CI phenaglycodol Scheme 1 (1) Identify the electrophile and nucleophile present in Step 1 (2 marks) (1) Draw the structure of Compound A (2 marks) (111) Identify reagent...
please do answer all the questions below. thank you
For each of the following complexes, draw the molecular structure and determine the effective atomic numbers. (i) Na[Fe(CN)s(NH3)3l (i) [Cr(H2O)2(NH3)2(en)]Cl (ii) [Co(o-phen)2(NHs)(NCS))CI (iv) (n3-C3Hs)Co(CO)2] (v) [Fe(diphos)(CO)sl in which diphos Ph2PCH2CH2PPh2 and Ph CsHs (10 marks) (i)/ The K for Fe(OH)4]2-is found to be higher than that found in (5 marks) Zn(OH)4]2-and [Cr(OHM. Explain . Cho and coworkers used the following ligand to react with cobalt. Predict how this ligand would bind...
please help in all questions!!
Which of the molecules below is the expected major product of the following reduction? Na, NH3) Н H Н нн H H For the given compounds answer the following. Compound A Compound B Compound C Identify which compound is expected to be most acidic. Compound A Compound B Compound C Choose the correct option to justify your choice. ODeprotonation of the compound generates an antiaromatic lon. Deprotonation of the compound generates an aromatic ion. Deprotonation...
Mechanisms. (2) For each experimental result shown below, propose a step-by-step "electron-pushing" mechanism, using "curly arrows". Show all intermediates (if there are any) explicitly. (a) HCI CI (b) н" +CH OH OCH, OH
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