Homework Answers
There are many questions in this post. I am answering subaprts a-d of the first question only (HOMEWORKLIB POLICY: 1 questions per post or 4 sub parts in 1 question)
ANSWER Q-5:
Part (a)
- CN- is a strong nucleophile and Br- is a great leaving group, then:
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Part (b)
- EtO- is a strong nucleophile and TsO- is a great leaving group, then:
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Part (c)
- Thiols are good nucleophiles and Br- i is a great leaving group, then:
---------------------------------------------------
Part (d)
- Aromatic compounds does not react by SN2 mechanism: then:
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how do i find the major product and fill out the
worksheet
help asap
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please explain the work for both questions please 1. Predict the major organic product for each...
please explain the work for both questions please
1. Predict the major organic product for each of the following elimination reactions, and indicate whether each one occurs via the E1 or the E2 mechanism. Be sure to clearly indicate the proper stereochemical relationships between groups (if appropriate), and write the word “racemic” under any compound that is formed as a racemic mixture. Br AgNO3 H2O KOt-Bu H3CCH3 H36Br t-BuOH OTS NaOCH3 CH3OH CH3 NaOH H20 2. Draw all possible E2...
confused on these reactions 01. Fill in the boxes with the product(s) for the following reactions. Draw only the pr...
confused on these reactions
01. Fill in the boxes with the product(s) for the following reactions. Draw only the predominate regioisomer and indicate the stereochemistry where appropriate. If a racemic mixture is formed, you may indicate this using a wavy line or mark the chiral center with an asterisk (*). and write racemic in the box. H NaOH, H2O 3) H0 NaOH, H2O in the boxes with the products for the following reactions. Draw only the predominate copioisomer and indicate...
please explain the work 1. Predict the major organic product for each of the following elimination...
please explain the work
1. Predict the major organic product for each of the following elimination reactions, and indicate whether each one occurs via the E1 or the E2 mechanism. Be sure to clearly indicate the proper stereochemical relationships between groups (if appropriate), and write the word "racemic" under any compound that is formed as a racemic mixture. Br H3CY CH3 NaOCH3. CH3OH OH يلي H2SO4 ما H3c OTS KOt-Bu t-BuOH AgNO3 H20 Ph HC, NaOH H2O OH H2SO4
1. A) Show each possible product for the reaction below and predict the major product. Be...
1. A) Show each possible product for the reaction below and predict the major product. Be sure. to include all geometric isomers. (1 pt) b Na B) Draw the rotamer that leads to the major product for the reaction above as a Newman projection. (1 pt) 2. Circle the substrates which can undergo elimination through the E2 mechanism. (Hint: substrates may not be drawn in the proper conformation for an E2 reaction). (0.5 pts) to x Kto 3. Circle the...
can you help me explain these especially number 2 Predict the major organic product for each...
can you help me explain these especially number 2
Predict the major organic product for each of the following elimination reactions, and indicate 1. whether each one occurs via the E1 or the E2 mechanism. Be sure to clearly indicate the proper stereochemical relationships between groups (if appropriate), and write the word "racemic" under any compound that is formed as a racemic mixture. g. Br AgNO3 Нао h. HасСНз KOt-Bu Hас Br t-BuOH ф- Draw all possible E2 products (including...
please help! Draw 2 major products Draw 1 minor product Turn your answer in BEFORE the next lecture. Late submission...
please help!
Draw 2 major products Draw 1 minor product Turn your answer in BEFORE the next lecture. Late submission will not be accepted. Scratch paper and scanned copy will not be accepted. Reaction type Reaction type Is the major products mixture optically active? (write yes or no) Draw 1 product Hea NaSCHE DMSO Q. Provide the reaction product(s). and indicate the type of reactions (SN 1. SN 2, E1 and E2) in the round rectangle. If reaction does not...
organic chemistry HELP ASAP! Fill in the boxes with the reagents, or major organic product(s) you...
organic chemistry HELP ASAP!
Fill in the boxes with the reagents, or major organic product(s) you would expect. Make sure to properly indicate the stereochemistry of the product(s) and indicate all stereoisomers formed 1) Mg. Et20 Br 2) PhCHO OH PCC 3) H30t 1) HB(Sia)2 2) NaOH H202 3) NaBH4 1) Mg. Et20 Br 2) PhCO2CH3 3) H30 DMSO (COCI)2 OH EtaN, CH2Cl2 1) Mg. Et2O 2) O 1) OsO4 H202 OH 3) H3o 2) PCC
Need help, numbers 3-6 please show work. and fill out table of chemicals for all chemical...
Need help, numbers 3-6 please show work. and fill out table of
chemicals for all chemical used.
calculate mmol in the table as well show work please
and each of these must be listed in its own row. There are 10 column headings: IUPAC name OR common name, structure, CAS number (Chemical Abstract Service number) molecular mass, melting point (if applicable), boiling point (if applicable), solubility (in water, if applicable), density, amounts to be used in the experiment, and the...
please explain the work for both questions please
1. Predict the major organic product for each of the following elimination reactions, and indicate whether each one occurs via the E1 or the E2 mechanism. Be sure to clearly indicate the proper stereochemical relationships between groups (if appropriate), and write the word “racemic” under any compound that is formed as a racemic mixture. Br AgNO3 H2O KOt-Bu H3CCH3 H36Br t-BuOH OTS NaOCH3 CH3OH CH3 NaOH H20 2. Draw all possible E2...
confused on these reactions
01. Fill in the boxes with the product(s) for the following reactions. Draw only the predominate regioisomer and indicate the stereochemistry where appropriate. If a racemic mixture is formed, you may indicate this using a wavy line or mark the chiral center with an asterisk (*). and write racemic in the box. H NaOH, H2O 3) H0 NaOH, H2O in the boxes with the products for the following reactions. Draw only the predominate copioisomer and indicate...
please explain the work
1. Predict the major organic product for each of the following elimination reactions, and indicate whether each one occurs via the E1 or the E2 mechanism. Be sure to clearly indicate the proper stereochemical relationships between groups (if appropriate), and write the word "racemic" under any compound that is formed as a racemic mixture. Br H3CY CH3 NaOCH3. CH3OH OH يلي H2SO4 ما H3c OTS KOt-Bu t-BuOH AgNO3 H20 Ph HC, NaOH H2O OH H2SO4
1. A) Show each possible product for the reaction below and predict the major product. Be sure. to include all geometric isomers. (1 pt) b Na B) Draw the rotamer that leads to the major product for the reaction above as a Newman projection. (1 pt) 2. Circle the substrates which can undergo elimination through the E2 mechanism. (Hint: substrates may not be drawn in the proper conformation for an E2 reaction). (0.5 pts) to x Kto 3. Circle the...
can you help me explain these especially number 2
Predict the major organic product for each of the following elimination reactions, and indicate 1. whether each one occurs via the E1 or the E2 mechanism. Be sure to clearly indicate the proper stereochemical relationships between groups (if appropriate), and write the word "racemic" under any compound that is formed as a racemic mixture. g. Br AgNO3 Нао h. HасСНз KOt-Bu Hас Br t-BuOH ф- Draw all possible E2 products (including...
please help!
Draw 2 major products Draw 1 minor product Turn your answer in BEFORE the next lecture. Late submission will not be accepted. Scratch paper and scanned copy will not be accepted. Reaction type Reaction type Is the major products mixture optically active? (write yes or no) Draw 1 product Hea NaSCHE DMSO Q. Provide the reaction product(s). and indicate the type of reactions (SN 1. SN 2, E1 and E2) in the round rectangle. If reaction does not...
organic chemistry HELP ASAP!
Fill in the boxes with the reagents, or major organic product(s) you would expect. Make sure to properly indicate the stereochemistry of the product(s) and indicate all stereoisomers formed 1) Mg. Et20 Br 2) PhCHO OH PCC 3) H30t 1) HB(Sia)2 2) NaOH H202 3) NaBH4 1) Mg. Et20 Br 2) PhCO2CH3 3) H30 DMSO (COCI)2 OH EtaN, CH2Cl2 1) Mg. Et2O 2) O 1) OsO4 H202 OH 3) H3o 2) PCC
Need help, numbers 3-6 please show work. and fill out table of
chemicals for all chemical used.
calculate mmol in the table as well show work please
and each of these must be listed in its own row. There are 10 column headings: IUPAC name OR common name, structure, CAS number (Chemical Abstract Service number) molecular mass, melting point (if applicable), boiling point (if applicable), solubility (in water, if applicable), density, amounts to be used in the experiment, and the...
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