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2) Draw all non-hydrogen substituents in the axial position for the following compound: он но он...
Please make sure to circle all non-hydrogen subtituents that are in axil position! Thanks! 4. For...
Please make sure to circle all non-hydrogen subtituents that are
in axil position! Thanks!
4. For each compound below, draw the most stable chair conformation. Do no draw in the hydrogen atoms. For clarity, circle all non-hydrogen substituents that are in an axial position. It may help to number the carbons in each chair first before drawing in each substituent. (3pts for each correct conformation properly drawn)
please answer all parts. your the best :) 4. For each compound below, draw the most...
please answer all parts. your the best :)
4. For each compound below, draw the most stable chair conformation. Do no draw in the hydrogen atoms. For clarity, circle all non-hydrogen substituents that are in an axial position. It may help to number the carbons in each chair first before drawing in cach substituent. (3pts for each correct conformation properly drawn) 5. (a) Convert Compound A (shown below) to its chair-like structure by placing the substituents of this compound in...
1) Circle all of the following compounds that is (are) primary alcohols он HO OH 2)...
1) Circle all of the following compounds that is (are) primary alcohols он HO OH 2) Write the IUPAC of the following compound Но, 3) Write the common name of the following compound Vo 4) Circle the following compounds that has the highest boiling point + oH OH HOMOH 5) Circle which of the following would be a reasonable synthesis of 1-butanol но- H2O 1. BH/THE 2. H2O2. HO H2O H2O 1. BH/THF 2. H2O2, HO
Compound E: C7H6O3 Hi, can someone please help me with the following questions? Draw a molecule...
Compound E: C7H6O3
Hi, can someone please help me with the following questions?
Draw a molecule that combines both of the above fragments. Show ALL hydrogen What is the molecular formula of the molecule you just drew? (Use the following format: CXHYOZ, where X, Y, and Z are numbers.) What is the molecular formula of the molecule you just drew? (Use the following format: CXHYOZ, where X, Y, and Z are numbers.) The difference between the formula you just wrote...
EXPERIMENT 4 Organic Families - Reactions and Identification of Functional Groups PART A. Reactions of Alkanes and Alkenes 1. Action of Bromine Water Observation Organic Compound cyclohexene c...
EXPERIMENT 4 Organic Families - Reactions and Identification of Functional Groups PART A. Reactions of Alkanes and Alkenes 1. Action of Bromine Water Observation Organic Compound cyclohexene cyclohexane Equations: Write an equation for the above compounds which caused a decolourisation of bromine water. Name and draw all reactants and products. Distinguishing Test for Primary, Secondary and Tertiary Alcohols PART B. 1. Lucas Test for Alcohols Organic Compound tert-pentanol (2-methyl 2-butanol) 2-pentanol Observation 1-pentanol Equations: Write an equation for the above...
Complete the structure below for the compound (2R. 3S)-3-amino-2-pentanol. Keeping the position of the amino and...
Complete the structure below for the compound (2R. 3S)-3-amino-2-pentanol. Keeping the position of the amino and hydroxy groups the same, draw a diastereomer of the compound you drew in part a. Write the top view for all stereoisomers of 1,2,3-trimethylcyclopentane (draw the cyclopentane ring in the plane of the paper). Clearly draw each stereoisomer using wedges and dashed bonds. You will lose credit for any duplications! Draw a 3-D orbital picture for the ethyl carbocalion. showing both carbon atoms in...
Draw the ringed (Haworth) structure of a-D-glucose below with proper numbering of carbons and all hydrogen...
Draw the ringed (Haworth) structure of a-D-glucose below with
proper numbering of carbons and all hydrogen group shown:
Question 1 (6 pts): Draw the ringed (Haworth) structure of a-D-glucose below with proper numbering of carbons and all hydrogen groups shown: aV Question 2 (3 pts): Fill in the blanks: In your above molecule, the B form of D-glucose would have the group at carbon position pointing in the direction. Question 3 (3 pts): Explain why we can easily digest potato...
QUESTIONS 1. Draw 2 different skeletal isomers of C7H16. 2. Draw 2 different functional isomers of C3H8O. 3. Compare th...
QUESTIONS 1. Draw 2 different skeletal isomers of C7H16. 2. Draw 2 different functional isomers of C3H8O. 3. Compare the information given by molecular formulas, structural formulas, and molecular models. 4. Why wouldn't CH3CH2CH2CH2CH2CH2CH2CH3 turn out as a straight line if you were to build the model? 5. State the molecular geometry for each of the following: a. a central carbon that has 4 single bonds b. a central carbon that has one double bond and two single bonds 6....
please answer all. I will rate thanks! (Review Topics) (References Classify the following substituents according to...
please answer all. I will rate thanks!
(Review Topics) (References Classify the following substituents according to whether they are electron donors or electron acceptors relative to hydrogen by the resonance and the inductive mechanisms. a = acceptor d = donor n = no effect Resonance effect :0: Inductive effect -CH=CH-C-GCH, 2. -=NCH3)2 Inductive effect :o: Inductive effect -CH2CH2CH2C-OCHE Resonance effect Resonance effect Submit Answer Retry Entire Group 9 more group attempts remaining Inductive effect Resonance effect CH3 2. :o: -c-ÖCH,CH,...
Be sure to answer all parts. Draw the enantiomer and a diastereomer for the following compound....
Be sure to answer all parts.
Draw the enantiomer and a diastereomer for the following
compound. (I got the diastereomer wrong)
Be sure to answer all parts. Draw the enantiomer and a diastereomer for the following compound. HO HO OH OH OH OH edit structure.. edit structure.. 2 Enantiomer Diastereomer Feedback When drawing an enantiomer, be sure you have drawn a non- superimnposable mirror image When drawing a diastereomer, check to see that one stereogenic center is different from the...
Please make sure to circle all non-hydrogen subtituents that are
in axil position! Thanks!
4. For each compound below, draw the most stable chair conformation. Do no draw in the hydrogen atoms. For clarity, circle all non-hydrogen substituents that are in an axial position. It may help to number the carbons in each chair first before drawing in each substituent. (3pts for each correct conformation properly drawn)
please answer all parts. your the best :)
4. For each compound below, draw the most stable chair conformation. Do no draw in the hydrogen atoms. For clarity, circle all non-hydrogen substituents that are in an axial position. It may help to number the carbons in each chair first before drawing in cach substituent. (3pts for each correct conformation properly drawn) 5. (a) Convert Compound A (shown below) to its chair-like structure by placing the substituents of this compound in...
1) Circle all of the following compounds that is (are) primary alcohols он HO OH 2) Write the IUPAC of the following compound Но, 3) Write the common name of the following compound Vo 4) Circle the following compounds that has the highest boiling point + oH OH HOMOH 5) Circle which of the following would be a reasonable synthesis of 1-butanol но- H2O 1. BH/THE 2. H2O2. HO H2O H2O 1. BH/THF 2. H2O2, HO
Compound E: C7H6O3
Hi, can someone please help me with the following questions?
Draw a molecule that combines both of the above fragments. Show ALL hydrogen What is the molecular formula of the molecule you just drew? (Use the following format: CXHYOZ, where X, Y, and Z are numbers.) What is the molecular formula of the molecule you just drew? (Use the following format: CXHYOZ, where X, Y, and Z are numbers.) The difference between the formula you just wrote...
EXPERIMENT 4 Organic Families - Reactions and Identification of Functional Groups PART A. Reactions of Alkanes and Alkenes 1. Action of Bromine Water Observation Organic Compound cyclohexene cyclohexane Equations: Write an equation for the above compounds which caused a decolourisation of bromine water. Name and draw all reactants and products. Distinguishing Test for Primary, Secondary and Tertiary Alcohols PART B. 1. Lucas Test for Alcohols Organic Compound tert-pentanol (2-methyl 2-butanol) 2-pentanol Observation 1-pentanol Equations: Write an equation for the above...
Complete the structure below for the compound (2R. 3S)-3-amino-2-pentanol. Keeping the position of the amino and hydroxy groups the same, draw a diastereomer of the compound you drew in part a. Write the top view for all stereoisomers of 1,2,3-trimethylcyclopentane (draw the cyclopentane ring in the plane of the paper). Clearly draw each stereoisomer using wedges and dashed bonds. You will lose credit for any duplications! Draw a 3-D orbital picture for the ethyl carbocalion. showing both carbon atoms in...
Draw the ringed (Haworth) structure of a-D-glucose below with
proper numbering of carbons and all hydrogen group shown:
Question 1 (6 pts): Draw the ringed (Haworth) structure of a-D-glucose below with proper numbering of carbons and all hydrogen groups shown: aV Question 2 (3 pts): Fill in the blanks: In your above molecule, the B form of D-glucose would have the group at carbon position pointing in the direction. Question 3 (3 pts): Explain why we can easily digest potato...
QUESTIONS 1. Draw 2 different skeletal isomers of C7H16. 2. Draw 2 different functional isomers of C3H8O. 3. Compare the information given by molecular formulas, structural formulas, and molecular models. 4. Why wouldn't CH3CH2CH2CH2CH2CH2CH2CH3 turn out as a straight line if you were to build the model? 5. State the molecular geometry for each of the following: a. a central carbon that has 4 single bonds b. a central carbon that has one double bond and two single bonds 6....
please answer all. I will rate thanks!
(Review Topics) (References Classify the following substituents according to whether they are electron donors or electron acceptors relative to hydrogen by the resonance and the inductive mechanisms. a = acceptor d = donor n = no effect Resonance effect :0: Inductive effect -CH=CH-C-GCH, 2. -=NCH3)2 Inductive effect :o: Inductive effect -CH2CH2CH2C-OCHE Resonance effect Resonance effect Submit Answer Retry Entire Group 9 more group attempts remaining Inductive effect Resonance effect CH3 2. :o: -c-ÖCH,CH,...
Be sure to answer all parts.
Draw the enantiomer and a diastereomer for the following
compound. (I got the diastereomer wrong)
Be sure to answer all parts. Draw the enantiomer and a diastereomer for the following compound. HO HO OH OH OH OH edit structure.. edit structure.. 2 Enantiomer Diastereomer Feedback When drawing an enantiomer, be sure you have drawn a non- superimnposable mirror image When drawing a diastereomer, check to see that one stereogenic center is different from the...
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