Answer questions A-D please. ONLY ANSWER THE QUESTIONS IF YOU KNOW IT FOR SURE BECAUSE MY MONEY IS BEING WASTED WHEN MY QUESTIONS ARE BEING ANSWERED WRONG. Thank you!!!
A.) Below is a summary of alkene reactions. Complete
them by providing the missing structures (including stereochemistry
wherever it applies).
B.) Draw the structure of the carbocation formed
during the reaction of the alkene from chart A with HCl.
C.) Draw the mechanism of the reaction of Br2 addition.
D.) Draw the mechanism of the reaction of Br2 addition with the
free radical initiator tBu-O-O-tBu.
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Answer questions A-D please. ONLY ANSWER THE QUESTIONS
IF YOU KNOW IT FOR SURE BECAUSE MY...
Starting from 3-methylhex-1-ene as the substrate at the center of your page, draw a reaction map showing the regiochemical and stereochemical outcome or outcomes for each of the following series of reagents. Name each of your products, including stereoche
Starting from 3-methylhex-1-ene as the substrate at the center of your page, draw a reaction map showing the regiochemical and stereochemical outcome or outcomes for each of the following series of reagents. Name each of your products, including stereochemical designations for any chirality centers that are generated.**Pay attention to the possibility of rearrangement when your mechanism produces a carbocation. A. H2SO4, H2OB. 1. Hg(OAc)2, H2O; 2. NaBH4C. 1. BH3•THF; 2. H2O2, NaOHD. Br2, CCl4E. Br2, H2OF. HBrG. HBr, ROORH. 1. O3; 2. DMSI. H2, Pt
can someone please answer this? thank you! For each reaction shown below, identify the primary product....
can
someone please answer this? thank you!
For each reaction shown below, identify the primary product. B regiochemistry and stereochemistry if applicable. Br2, H2O KMnO4, NaOH cold 1. Hg(OAc)2, H2O 2. NABH4 1. O3 2. Zn/ACOH 1. BH3 2. H-О, NaOH Cl2 Write the mechanism of the first reaction, the bromohydrin r
Acid Catalyzed Hydration-treatment of alkenes with water in the presence of acid catalyst leads to the...
Acid Catalyzed Hydration-treatment of alkenes with water in the presence of acid catalyst leads to the formation of alcohols. H2SO4/H2O > 150°C Mechanism Major Product Acid catalyzed dehydration goes through a carbocation intermediate. This means that the Markovnikov product is obtained when carbocation rearrangements do not occur. The need for excessively high temperatures makes this reaction of limited use in laboratory synthesis. Oxymercuration - Oxymercuration involves the addition of Hg to the alkene using mercury (II) acetate Hg(OAc) followed by...
Please include the mechanism In each reaction box, place the best reagent and conditions from the...
Please include the mechanism
In each reaction box, place the best reagent and conditions from the list below. CEOY bromocyclohexane H2O, NaOH, H,O H, Lindlar catalyst excess NaNH2, then H2O 2 equiv. NaNH2 CH3Br SOCI H20, H2SO4, HgSO4 CH3CH2B1 NaBH4 BHYTHF НВК Br2
Hello! Just double checking the answers my organic chemistry study guide. Please go ahead and answer ALL the questions you see below, if you can't answer all then PLEASE let someone else do them!...
Hello! Just double checking the answers my organic chemistry
study guide. Please go ahead and answer ALL the
questions you see below, if you can't answer all then
PLEASE let someone else do them! High rating only
given to ALL questions complete
21. Provide reagents (including solvent and/or special conditions, such as light) to complete the following reaction scheme. CH3-CCH-CH2 CH3 H3C CO+Ho -CH CH OH Page 8 of 9 HC H3C gOCH2CH3 18. Draw the structure of the alkene...
s) Predict the principal organic product(s) in each of the following reactions. Draw the correct stereoisom...
s) Predict the principal organic product(s) in each of the following reactions. Draw the correct stereoisom wherever applicable (Structures with incomplete/wrong stereochemistry will not be accepted!!). CH₃ Clz Br2 Н,0 CCIA 1) BH3. THE 2) H2Oz/NaOH 1) O₃ 2) (CH3)2S МСРВА MCPECIES CH2Cl2 OsO4 NMO 1) МСРВА 2) H2O/H30* Hoy for Hos 1) Brz/H20 2) NaOH 1) Hg(OAC)2, H2O/THF 2) NaBHA = 1) O₃ 2) H20 340 H2SO4 HgSO4 2 Brz CCIA 2 HCI 26. pts) Listed below is information...
home / study / science / chemistry / chemistry questions and answers / hello! just double checking the answers my organic chemistry study guide. please go ahead and ... Question: Hello! Just double ch...
home / study / science / chemistry / chemistry questions and
answers / hello! just double checking the answers my organic
chemistry study guide. please go ahead and ...
Question: Hello! Just double checking the answers my
organic chemistry study guide. Please go ahead and ans...
Hello! Just double checking the answers my organic chemistry
study guide. Please go ahead and answer ALL the
questions you see below, if you can't answer all then
PLEASE let someone else do them!...
Answer the following two questions about the following synthetic scheme. (Numbers in parentheses below the structures...
Answer the following two questions about the following synthetic scheme. (Numbers in parentheses below the structures are for identification purposes.) CH, Cl/h CI KOH CI +K -HCI - H2O NO2 NO NO2 (1) (2) (3) CA NO2 NO2 NO2 -KCI -HCI CI (4) (5) NO, NO H/Pd/C A NH2 -NH (6) (7) NH2 Br + (9) (8) ta +NH -HCI -HCI CI HAN (10) What is the role of KOH in the conversion of 2) to (3)? Select one: O...
List Notes You may attempt this question 4 more times for credit Score: Sorry, you are...
List Notes You may attempt this question 4 more times for credit Score: Sorry, you are incorrect Answer(s): (Your response(s) are shown below.) Question 8.33 em tion The acid-catalyzed addition of alcohols to alkenes occurs via a mechanism analogous to acid-catalyzed alkene hydration. The reaction occurs in 3 1) Addition of H to the alkene, together with any possible carbocation rearrangements: 2) Addition of the alcohol to the carbocation: 3) Deprotonation to yield the product ether ation sage tages Draw...
Please help look this over I just want to double check my answer! thanks! Critical Thinking...
Please help look this over I just want to double check my
answer! thanks!
Critical Thinking Questions: 2) The polymerization of ethylene ("monomer") with a radical initiator follows the same chain reaction. Please write the mechanism (all arrows) from ethylene (==ethene) to polyethylene). Start with an initiator of R-R. After breaking the initiator bond to your radicals, use either radical for your 1"' reaction with ethylene. Indicate repeating reactions by multiple arrows. Write the final product in a common short...
can
someone please answer this? thank you!
For each reaction shown below, identify the primary product. B regiochemistry and stereochemistry if applicable. Br2, H2O KMnO4, NaOH cold 1. Hg(OAc)2, H2O 2. NABH4 1. O3 2. Zn/ACOH 1. BH3 2. H-О, NaOH Cl2 Write the mechanism of the first reaction, the bromohydrin r
Acid Catalyzed Hydration-treatment of alkenes with water in the presence of acid catalyst leads to the formation of alcohols. H2SO4/H2O > 150°C Mechanism Major Product Acid catalyzed dehydration goes through a carbocation intermediate. This means that the Markovnikov product is obtained when carbocation rearrangements do not occur. The need for excessively high temperatures makes this reaction of limited use in laboratory synthesis. Oxymercuration - Oxymercuration involves the addition of Hg to the alkene using mercury (II) acetate Hg(OAc) followed by...
Please include the mechanism
In each reaction box, place the best reagent and conditions from the list below. CEOY bromocyclohexane H2O, NaOH, H,O H, Lindlar catalyst excess NaNH2, then H2O 2 equiv. NaNH2 CH3Br SOCI H20, H2SO4, HgSO4 CH3CH2B1 NaBH4 BHYTHF НВК Br2
Hello! Just double checking the answers my organic chemistry
study guide. Please go ahead and answer ALL the
questions you see below, if you can't answer all then
PLEASE let someone else do them! High rating only
given to ALL questions complete
21. Provide reagents (including solvent and/or special conditions, such as light) to complete the following reaction scheme. CH3-CCH-CH2 CH3 H3C CO+Ho -CH CH OH Page 8 of 9 HC H3C gOCH2CH3 18. Draw the structure of the alkene...
s) Predict the principal organic product(s) in each of the following reactions. Draw the correct stereoisom wherever applicable (Structures with incomplete/wrong stereochemistry will not be accepted!!). CH₃ Clz Br2 Н,0 CCIA 1) BH3. THE 2) H2Oz/NaOH 1) O₃ 2) (CH3)2S МСРВА MCPECIES CH2Cl2 OsO4 NMO 1) МСРВА 2) H2O/H30* Hoy for Hos 1) Brz/H20 2) NaOH 1) Hg(OAC)2, H2O/THF 2) NaBHA = 1) O₃ 2) H20 340 H2SO4 HgSO4 2 Brz CCIA 2 HCI 26. pts) Listed below is information...
home / study / science / chemistry / chemistry questions and
answers / hello! just double checking the answers my organic
chemistry study guide. please go ahead and ...
Question: Hello! Just double checking the answers my
organic chemistry study guide. Please go ahead and ans...
Hello! Just double checking the answers my organic chemistry
study guide. Please go ahead and answer ALL the
questions you see below, if you can't answer all then
PLEASE let someone else do them!...
Answer the following two questions about the following synthetic scheme. (Numbers in parentheses below the structures are for identification purposes.) CH, Cl/h CI KOH CI +K -HCI - H2O NO2 NO NO2 (1) (2) (3) CA NO2 NO2 NO2 -KCI -HCI CI (4) (5) NO, NO H/Pd/C A NH2 -NH (6) (7) NH2 Br + (9) (8) ta +NH -HCI -HCI CI HAN (10) What is the role of KOH in the conversion of 2) to (3)? Select one: O...
List Notes You may attempt this question 4 more times for credit Score: Sorry, you are incorrect Answer(s): (Your response(s) are shown below.) Question 8.33 em tion The acid-catalyzed addition of alcohols to alkenes occurs via a mechanism analogous to acid-catalyzed alkene hydration. The reaction occurs in 3 1) Addition of H to the alkene, together with any possible carbocation rearrangements: 2) Addition of the alcohol to the carbocation: 3) Deprotonation to yield the product ether ation sage tages Draw...
Please help look this over I just want to double check my
answer! thanks!
Critical Thinking Questions: 2) The polymerization of ethylene ("monomer") with a radical initiator follows the same chain reaction. Please write the mechanism (all arrows) from ethylene (==ethene) to polyethylene). Start with an initiator of R-R. After breaking the initiator bond to your radicals, use either radical for your 1"' reaction with ethylene. Indicate repeating reactions by multiple arrows. Write the final product in a common short...
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