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need help asap qs 24 and 25, thank you
24. Write the mechanism for the reaction...
I need help determining the reagents needed for these reactions. Part 5. Draw the mechanism. Draw...
I need help determining the reagents needed for these
reactions.
Part 5. Draw the mechanism. Draw the mechanism for each of the following reactions shown below. Be sure to show all steps in the reaction, the intermediates formed at each step, and use curved arrows to track the flow of electrons (20 pts) H2SO4 OH H6-3-sit GO Draw your mechanism below: 4 o Acid so ontsler deprotonation first step 12 000 BP2 + HBO Draw your mechanism below: +HBO, +H-Br
help with page 23. How is the following step in the free radical chlorination mechanism described...
help with page
23. How is the following step in the free radical chlorination mechanism described *CH3 + 'Cl → CHCI a. initiation step b . termination step c. propagation step d. electrophilic step 24. Which compound would give the following alkene as the major product in an elimination reaction with CH3CH2ONat? ? CHỊCHONa. Br Br 1 3 a. 1 b. 2 c. 3 d. 1 and 3 25. What is the product of the following reaction? OH H2SO4 он...
i need help with these synthesis problems: a,b,c 3) Show how the following molecules can be synthesized from the sta...
i need help with these synthesis problems: a,b,c
3) Show how the following molecules can be synthesized from the starting material indicated. Draw the structure of each intermediary compound in your synthesis, and add reagents above/beneath your reaction arrows. (24 points total). CHO HOH CHO HOH H -OH H-OH HOH H- OH НТОН CH OM CH OH DOH Cros Co ^Nitz DEN ĮHz, Pd-c 17 -NO₂ Page 3 of 5
Please answer ASAP!! will rate! thank you Part A Write the chemical equation for the reduction...
Please answer ASAP!! will rate! thank
you
Part A Write the chemical equation for the reduction of acetaldehyde to ethanol. Complete the reaction by dragging the appropriate labels to their respective targets. Note: not all labels will be used. Reset Help OH CH;-(-OH CO2 + NADH NAD NADH + H Hz-CH2-C- CH3-C-H HS - COA + NAD+ CH3-C-C-H (coenzyme) (coenzyme)
I need help answering these questions, I appreciate your help in this difficult time! En route...
I need help answering these questions, I appreciate your help in
this difficult time!
En route to vitamin B1, this acid catalyzed dehydration reaction occurs. Provide a step by step mechanism along with the structure of the product. Hint: the product has a CN double bond. HEN HOCHSH IN-H- - Under dehydrating conditions, alpha-terpineol, a major constituent of pine oil, forms three unique dienes, each with a particular scent. Provide the missing cationic intermediates. Note: no curved arrows needed, but...
Hello, please help me figure out the mechanism for this reaction. Thank you! r.t., 24 h r.t., 24 h
Hello, please help me figure out the mechanism for this
reaction. Thank you!
r.t., 24 h
r.t., 24 h
please help!! thank you! Which of the following compounds is most reactive towards nucleophilic addition reaction?...
please help!! thank you!
Which of the following compounds is most reactive towards nucleophilic addition reaction? H1 H H A B С D E Predict the product for the following reaction sequence. iii PBrz Mg/ether Н H Cr04 ОН 2. Hz0+ A. 6,7-dimethyl-3-nonanol B. 6,7-dimethyl-3-nonanone C. 6,7-dimethyl-3-nonanal D. 3,4-dimethyl-7-nonanol E. 3,4-dimethyl-7-nonanone Predict the product for the following reaction 1. LiAlH4 (excess) 2. H30* OH OH OH -Н HO B с D Provide the structure of the ylide needed to prepare...
i need help asap. thank you 2 From the following structures, provide a correct name for...
i
need help asap. thank you
2 From the following structures, provide a correct name for the following organic molecules (be sure to include stereochemical prefixes where necessary) сн сн, сн, (a) осн, (b) CH (c) осн, (. н.со (e) (g) HO. (h) (k)
please help solve question 23, question 24 and question 25. thank you THE FOLLOWING SCHEME APPLIES...
please help solve question 23, question 24 and question 25.
thank you
THE FOLLOWING SCHEME APPLIES TO QUESTIONS 23, 24 AND 25 12 CH HECH CH3 HyCCHE (1) H, SO H2O (2) MCPBA CH2Cl2 (3) NaBH Ethanol OH OH QUESTION 23 [2] What, if at all, is wrong with step (1)? A B The product suggests acid catalyzed anti-Markovnikov addition of water to an alkene, which is not possible The reaction needs concentrated sulfuric acid, not its dilute water solution...
need help ASAP please and thank you. Give the IUPAC name for the following compound: CH3CH2CH(OH)CH,CH,CHOH...
need help ASAP please and thank you.
Give the IUPAC name for the following compound: CH3CH2CH(OH)CH,CH,CHOH 1 ,4 - hexanediol
I need help determining the reagents needed for these
reactions.
Part 5. Draw the mechanism. Draw the mechanism for each of the following reactions shown below. Be sure to show all steps in the reaction, the intermediates formed at each step, and use curved arrows to track the flow of electrons (20 pts) H2SO4 OH H6-3-sit GO Draw your mechanism below: 4 o Acid so ontsler deprotonation first step 12 000 BP2 + HBO Draw your mechanism below: +HBO, +H-Br
help with page
23. How is the following step in the free radical chlorination mechanism described *CH3 + 'Cl → CHCI a. initiation step b . termination step c. propagation step d. electrophilic step 24. Which compound would give the following alkene as the major product in an elimination reaction with CH3CH2ONat? ? CHỊCHONa. Br Br 1 3 a. 1 b. 2 c. 3 d. 1 and 3 25. What is the product of the following reaction? OH H2SO4 он...
i need help with these synthesis problems: a,b,c
3) Show how the following molecules can be synthesized from the starting material indicated. Draw the structure of each intermediary compound in your synthesis, and add reagents above/beneath your reaction arrows. (24 points total). CHO HOH CHO HOH H -OH H-OH HOH H- OH НТОН CH OM CH OH DOH Cros Co ^Nitz DEN ĮHz, Pd-c 17 -NO₂ Page 3 of 5
Please answer ASAP!! will rate! thank
you
Part A Write the chemical equation for the reduction of acetaldehyde to ethanol. Complete the reaction by dragging the appropriate labels to their respective targets. Note: not all labels will be used. Reset Help OH CH;-(-OH CO2 + NADH NAD NADH + H Hz-CH2-C- CH3-C-H HS - COA + NAD+ CH3-C-C-H (coenzyme) (coenzyme)
I need help answering these questions, I appreciate your help in
this difficult time!
En route to vitamin B1, this acid catalyzed dehydration reaction occurs. Provide a step by step mechanism along with the structure of the product. Hint: the product has a CN double bond. HEN HOCHSH IN-H- - Under dehydrating conditions, alpha-terpineol, a major constituent of pine oil, forms three unique dienes, each with a particular scent. Provide the missing cationic intermediates. Note: no curved arrows needed, but...
Hello, please help me figure out the mechanism for this
reaction. Thank you!
r.t., 24 h
r.t., 24 h
please help!! thank you!
Which of the following compounds is most reactive towards nucleophilic addition reaction? H1 H H A B С D E Predict the product for the following reaction sequence. iii PBrz Mg/ether Н H Cr04 ОН 2. Hz0+ A. 6,7-dimethyl-3-nonanol B. 6,7-dimethyl-3-nonanone C. 6,7-dimethyl-3-nonanal D. 3,4-dimethyl-7-nonanol E. 3,4-dimethyl-7-nonanone Predict the product for the following reaction 1. LiAlH4 (excess) 2. H30* OH OH OH -Н HO B с D Provide the structure of the ylide needed to prepare...
i
need help asap. thank you
2 From the following structures, provide a correct name for the following organic molecules (be sure to include stereochemical prefixes where necessary) сн сн, сн, (a) осн, (b) CH (c) осн, (. н.со (e) (g) HO. (h) (k)
please help solve question 23, question 24 and question 25.
thank you
THE FOLLOWING SCHEME APPLIES TO QUESTIONS 23, 24 AND 25 12 CH HECH CH3 HyCCHE (1) H, SO H2O (2) MCPBA CH2Cl2 (3) NaBH Ethanol OH OH QUESTION 23 [2] What, if at all, is wrong with step (1)? A B The product suggests acid catalyzed anti-Markovnikov addition of water to an alkene, which is not possible The reaction needs concentrated sulfuric acid, not its dilute water solution...
need help ASAP please and thank you.
Give the IUPAC name for the following compound: CH3CH2CH(OH)CH,CH,CHOH 1 ,4 - hexanediol
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