Please show all work! Thank you so much
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Please show all work! Thank you so much 4. (0.5pt) When a single compound contains both a nucleophile and a leav...
Click the "draw structure" button to launch the drawing utility. When a single compound contains both...
Click the "draw structure" button to launch the drawing utility. When a single compound contains both a nucleophile and a leaving group, an intramolecular reaction may occur. With this in mind, draw the product of the following reaction, including stereochemistry. OOHOO OH C7H1002 + Br V "Br + H2O + Br edit structure ...
Please help with both questions with all work shown (lone pairs, charges, arrows). Thank you so...
Please help with both questions with all work shown
(lone pairs, charges, arrows). Thank you so much!
(4pts) Draw the appropriate substrate and nucleophile needed to make the following compounds via S2 in the highest yield. SH (3pts) Identify the a carbon and B carbon(s) on the structures below. Provide the product(s) of an E2 reaction between the structure shown below and OC(CHs)a а. Cl oc(CHa) b. Br oC (CHs)s C. Br -OC cCH
Please show all work for Number 5: CH3OH and number 3, HF one. Thank you Complete...
Please show all work for
Number 5: CH3OH and number 3, HF one. Thank you
Complete the following reaction and provide forget resonance structures when applicable. a. a detailed arrow-pushing mechanism. Don't HF OH 5. (28 pt.) Complete the following reactions with the correct structures of starting material or product(s) Indicate 'major' and 'minor' if applicable. Don't forget to specify the stereochemistry and draw both enantiomers if applicable. Provide mechanism only if indicated. Cl2/H20 Et AV Use the provided template...
Please show all work and explanations if possible. Thank you so much! 4. (4pts) A mass spectrum shows significant pe...
Please show all work and explanations if possible.
Thank you so much!
4. (4pts) A mass spectrum shows significant peaks at m/z 87, 115, and 143. Which of the following compounds is responsible for that mass spectrum: 4,7-dimethyl-1-octanol, 2,6-dimethyl-4-octanol, or 2,2,4-trimethyl-4-heptanol? Provide structures of the cationic fragments that support your choice and provide the mechanism for the formation of ONE of these fragments from the molecular ion. он он но
PLEASE SHOW ALL WORK AND PLEASE ANSWER ALL PARTS OF EACH QUESTION! Thank you! 06 Question (4 points) e See page 574 Comp...
PLEASE SHOW ALL WORK AND
PLEASE ANSWER ALL PARTS OF EACH QUESTION! Thank you!
06 Question (4 points) e See page 574 Complete the mechanism. All necessary atoms and bonds (that is, those that are involved in the mechanism) are drawn in for you already; do not modify the structures by adding or removing any atoms. 1st attempt See Periodic Table See Hint Add the missing curved arrow notation. e See pa 09 Question (4 points) Predict the organic starting...
Please give detailed answers to the pre and post lab questions. Thank you! NUCLEOPHILIC DISPLACEMENT- FORMATION...
Please give detailed answers to the pre and post lab questions.
Thank you!
NUCLEOPHILIC DISPLACEMENT- FORMATION OF AN ETHER BY AN SN2 REACTION Bond formation by use of an SN2 reaction is very important for organic and biological synthesis. Many new bonds formed make use of this versatile reaction pathway. In this reaction, one partner is the nucleophile and the other partner is the electrophile. The electrophile will have a leaving group that will be lost in the reaction. In...
please need help with all the questions and ASAP, thank you 11. Please predict the principle...
please need help with all the questions and ASAP, thank you
11. Please predict the principle organic product of the following reactions, show stereochemistry where appropriate. Note that some reactions involve isotope-labeled compounds, in those cases the correct isotope must be used. (66') 1. LIAID 2. H,O (1) 18 1) THF (2). CH3Li + 2) HaO NaBH4 (3) CH3OD H2(excess)/Pt (4) d herd (5). - Mg Br D2O diethyl ether Br +Li (6) diethyl ether LICu(CH2CHs)2 Br (7). 1. diethyl...
please help with how the flow chart will look like? thank you! Synthesis of n-Butyl Bromide...
please help with how the flow chart will look like? thank
you!
Synthesis of n-Butyl Bromide Purpose of the Experiment: In this week's experiment you will be synthesizing n-butylbromide (IUPAC 1-bromobutane from 1-butanol and a concentrated acid via a nucleophilie substitution reaction. It is important to know that alcohols dehydrate to form alkenes in the presence of strong inorganic acids, so care must be taken in this experiment not to heat the reaction too vigorously else an elimination reaction may...
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...
Click the "draw structure" button to launch the drawing utility. When a single compound contains both a nucleophile and a leaving group, an intramolecular reaction may occur. With this in mind, draw the product of the following reaction, including stereochemistry. OOHOO OH C7H1002 + Br V "Br + H2O + Br edit structure ...
Please help with both questions with all work shown
(lone pairs, charges, arrows). Thank you so much!
(4pts) Draw the appropriate substrate and nucleophile needed to make the following compounds via S2 in the highest yield. SH (3pts) Identify the a carbon and B carbon(s) on the structures below. Provide the product(s) of an E2 reaction between the structure shown below and OC(CHs)a а. Cl oc(CHa) b. Br oC (CHs)s C. Br -OC cCH
Please show all work for
Number 5: CH3OH and number 3, HF one. Thank you
Complete the following reaction and provide forget resonance structures when applicable. a. a detailed arrow-pushing mechanism. Don't HF OH 5. (28 pt.) Complete the following reactions with the correct structures of starting material or product(s) Indicate 'major' and 'minor' if applicable. Don't forget to specify the stereochemistry and draw both enantiomers if applicable. Provide mechanism only if indicated. Cl2/H20 Et AV Use the provided template...
Please show all work and explanations if possible.
Thank you so much!
4. (4pts) A mass spectrum shows significant peaks at m/z 87, 115, and 143. Which of the following compounds is responsible for that mass spectrum: 4,7-dimethyl-1-octanol, 2,6-dimethyl-4-octanol, or 2,2,4-trimethyl-4-heptanol? Provide structures of the cationic fragments that support your choice and provide the mechanism for the formation of ONE of these fragments from the molecular ion. он он но
PLEASE SHOW ALL WORK AND
PLEASE ANSWER ALL PARTS OF EACH QUESTION! Thank you!
06 Question (4 points) e See page 574 Complete the mechanism. All necessary atoms and bonds (that is, those that are involved in the mechanism) are drawn in for you already; do not modify the structures by adding or removing any atoms. 1st attempt See Periodic Table See Hint Add the missing curved arrow notation. e See pa 09 Question (4 points) Predict the organic starting...
Please give detailed answers to the pre and post lab questions.
Thank you!
NUCLEOPHILIC DISPLACEMENT- FORMATION OF AN ETHER BY AN SN2 REACTION Bond formation by use of an SN2 reaction is very important for organic and biological synthesis. Many new bonds formed make use of this versatile reaction pathway. In this reaction, one partner is the nucleophile and the other partner is the electrophile. The electrophile will have a leaving group that will be lost in the reaction. In...
please need help with all the questions and ASAP, thank you
11. Please predict the principle organic product of the following reactions, show stereochemistry where appropriate. Note that some reactions involve isotope-labeled compounds, in those cases the correct isotope must be used. (66') 1. LIAID 2. H,O (1) 18 1) THF (2). CH3Li + 2) HaO NaBH4 (3) CH3OD H2(excess)/Pt (4) d herd (5). - Mg Br D2O diethyl ether Br +Li (6) diethyl ether LICu(CH2CHs)2 Br (7). 1. diethyl...
please help with how the flow chart will look like? thank
you!
Synthesis of n-Butyl Bromide Purpose of the Experiment: In this week's experiment you will be synthesizing n-butylbromide (IUPAC 1-bromobutane from 1-butanol and a concentrated acid via a nucleophilie substitution reaction. It is important to know that alcohols dehydrate to form alkenes in the presence of strong inorganic acids, so care must be taken in this experiment not to heat the reaction too vigorously else an elimination reaction may...
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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