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a.Fill in missing H-atoms, Cl-atoms, CH3 groups and OH groups
in the line structure. Assign the...
3) Which of the following compounds is chiral? A) H Н-С-н н B) H HO C-OH Н C) CH3 HO-C-H Cl D) Br Н-С-ОН н E) C B...
3) Which of the following compounds is chiral? A) H Н-С-н н B) H HO C-OH Н C) CH3 HO-C-H Cl D) Br Н-С-ОН н E) C Br- C-C Br 4) In the L- isomer of a Fischer projection of a monosaccharide, the -OH group furthest from the carbonyl is written A) on the left of the top chiral carbon B) on the right of the top chiral carbon C) on the left of the middle chiral carbon D) on...
1) Label the acidic functional groups 2) For each acidic site, indicate if it has been...
1) Label the acidic functional groups
2) For each acidic site, indicate if it has been drawn in the
protonated form or not
9/1/16 Name: Worksheet 2 Below is a partial structure of Humic Acid, Circle AND name SEVEN different functional groups on the molecule НООС HOOC сно нс-он COOH --0 он НО. но-сн НО он ( ОН нс-он COOH о HC-OH с=0 o- НО но оноо ОН HN NH
Draw the ammonium salt formed in each reaction. All atoms should be drawn Reaction A Modify...
Draw the ammonium salt formed in each reaction. All atoms should be drawn Reaction A Modify the structure to give the product of reaction A Draw the counterion More Select Draw Rings Erase CL C Н N НС CH CH НС H2 НС нс НС. CHз N н N CH H CHз сH, CI Modify the structure to give the product of reaction B Draw the counterion Reaction B Erase More Rings Draw Select N Н н, Н, сн, H2...
having trouble with R and S configuration, can someone help out with this sheet? 17 Br>Cl'7...
having trouble with R and S configuration, can someone help out
with this sheet?
17 Br>Cl'7 S"7 F>ONTO77i77 H 1. Determine the configuration (R or S) of each of the following molecules: (Ph phenyl, a benzene ring as a group) CH-CH3 b. CHs с. но NH2 d. он COOH Ph H Hас CH2CH3 H2N CH&CH NH2 NH2 f. Ph CH3 Ph CHs h. H i. OH c lCOOH н.сн,с F Н.с NH2 h. COOH CHs CH2CH H2N 2. Label the...
8. What is the major product of the following reaction? Cн, CH Cl (solvent) C сн, a сн, CH CH H OH H OH OH 9. What...
8. What is the major product of the following reaction? Cн, CH Cl (solvent) C сн, a сн, CH CH H OH H OH OH 9. What is the degree of unsaturation of C10H12N203? a 4 b.5 c. 6 d.7 10. Which of the following statement about using curved arrows in polar reaction mechanism is true? a. The nucleophile can be either negatively charged or positively charged. b. The electrophile must be neutral. c. Electrons move from a nucleophilic source...
What is the major product of the following reaction? Hy(excess) Lindlar's cat. A B D Ос...
What is the major product of the following reaction? Hy(excess) Lindlar's cat. A B D Ос B A D What is the major product of the following reaction? Cl2 Н,0 НО СІ. A \ Он С В с D CI CI ОН ОН Ов ОА D с What is the major product of the following reaction? CH3 нс Н сH,CH, NaNH2 DMSO Br А В CH3 CHCH3 9 CH3 с CH,CH H4C. D нс CH2CH3 CH3 "NH, нс Сн HECH...
Meet with your group to answer the following free-response problems. You may use any resources at...
Meet with your group to answer the following free-response problems. You may use any resources at your disposal. You may upload your answers as a photo or ChemDraw file. 9) Fischer Projections a) Convert the Fisher Projection a zig-zag structure by filling in the missing groups on the hashed/wedged structure below. Designate the configuration (D/L) of the Fisher Projection. (4 points) сно H+OCH HOH H+OH H+OH CH2OH OH Circle one: D or L b) Fill in the missing groups for...
What are the compound structures for #13-16? The IUPAC name! Compound Structure # Cl H H...
What are the compound structures for #13-16?
The IUPAC name!
Compound Structure # Cl H H Н Н—С —С—С—С—Н ннн СH3 СHs H F тI CH3 —С —С —с%3Dс Н 10 Н H F CH3 H CзH, н н IIII С3D С—С—С—С—С—CН; Н 11 Н ннн СНз Br Н—с—с—с— СH, 12 Cl Br СHs H СH3 Н Н CI—С —С —С —С—С%%3 С 13 Н CI HHCІ Н СН, н Н Н—с—с—С—с—Н 14 н нСН, н Нн F Н,С —...
draw your cyclic model by adding the OH groups and H atoms to figure below. le...
draw your cyclic model by adding the OH groups and H atoms to
figure below.
le the drawing a Unded black atom white atoms. Cl, use green For Br, use pe For all Lone chiral Cater b. Convert the open form of ribose into a eyelie form. Here's how: 1. Pull apart one of the Co bonds from the Catom, leaving the other end of the bond attached to the O atom. . Connect the free bond from the O...
2) Order the following alkenes from most stable to least stable Нас Нас с-сн, н,с Hас +C- Нас н CHs -CH3 H Hе mos...
2) Order the following alkenes from most stable to least stable Нас Нас с-сн, н,с Hас +C- Нас н CHs -CH3 H Hе most stable least stable (a) I (b) I (c) I ll (d) 7) Order the following C-H bonds from strongest to weakest. strongest weakest (a) (b) (c) II (d) 8) Which of the following is represents the lowest energy transition state for the addition of BH, to 2-methyl-1-propene? quCH «сHs нСи Нас (b) (a) Нив--н H H...
3) Which of the following compounds is chiral? A) H Н-С-н н B) H HO C-OH Н C) CH3 HO-C-H Cl D) Br Н-С-ОН н E) C Br- C-C Br 4) In the L- isomer of a Fischer projection of a monosaccharide, the -OH group furthest from the carbonyl is written A) on the left of the top chiral carbon B) on the right of the top chiral carbon C) on the left of the middle chiral carbon D) on...
1) Label the acidic functional groups
2) For each acidic site, indicate if it has been drawn in the
protonated form or not
9/1/16 Name: Worksheet 2 Below is a partial structure of Humic Acid, Circle AND name SEVEN different functional groups on the molecule НООС HOOC сно нс-он COOH --0 он НО. но-сн НО он ( ОН нс-он COOH о HC-OH с=0 o- НО но оноо ОН HN NH
Draw the ammonium salt formed in each reaction. All atoms should be drawn Reaction A Modify the structure to give the product of reaction A Draw the counterion More Select Draw Rings Erase CL C Н N НС CH CH НС H2 НС нс НС. CHз N н N CH H CHз сH, CI Modify the structure to give the product of reaction B Draw the counterion Reaction B Erase More Rings Draw Select N Н н, Н, сн, H2...
having trouble with R and S configuration, can someone help out
with this sheet?
17 Br>Cl'7 S"7 F>ONTO77i77 H 1. Determine the configuration (R or S) of each of the following molecules: (Ph phenyl, a benzene ring as a group) CH-CH3 b. CHs с. но NH2 d. он COOH Ph H Hас CH2CH3 H2N CH&CH NH2 NH2 f. Ph CH3 Ph CHs h. H i. OH c lCOOH н.сн,с F Н.с NH2 h. COOH CHs CH2CH H2N 2. Label the...
8. What is the major product of the following reaction? Cн, CH Cl (solvent) C сн, a сн, CH CH H OH H OH OH 9. What is the degree of unsaturation of C10H12N203? a 4 b.5 c. 6 d.7 10. Which of the following statement about using curved arrows in polar reaction mechanism is true? a. The nucleophile can be either negatively charged or positively charged. b. The electrophile must be neutral. c. Electrons move from a nucleophilic source...
What is the major product of the following reaction? Hy(excess) Lindlar's cat. A B D Ос B A D What is the major product of the following reaction? Cl2 Н,0 НО СІ. A \ Он С В с D CI CI ОН ОН Ов ОА D с What is the major product of the following reaction? CH3 нс Н сH,CH, NaNH2 DMSO Br А В CH3 CHCH3 9 CH3 с CH,CH H4C. D нс CH2CH3 CH3 "NH, нс Сн HECH...
Meet with your group to answer the following free-response problems. You may use any resources at your disposal. You may upload your answers as a photo or ChemDraw file. 9) Fischer Projections a) Convert the Fisher Projection a zig-zag structure by filling in the missing groups on the hashed/wedged structure below. Designate the configuration (D/L) of the Fisher Projection. (4 points) сно H+OCH HOH H+OH H+OH CH2OH OH Circle one: D or L b) Fill in the missing groups for...
What are the compound structures for #13-16?
The IUPAC name!
Compound Structure # Cl H H Н Н—С —С—С—С—Н ннн СH3 СHs H F тI CH3 —С —С —с%3Dс Н 10 Н H F CH3 H CзH, н н IIII С3D С—С—С—С—С—CН; Н 11 Н ннн СНз Br Н—с—с—с— СH, 12 Cl Br СHs H СH3 Н Н CI—С —С —С —С—С%%3 С 13 Н CI HHCІ Н СН, н Н Н—с—с—С—с—Н 14 н нСН, н Нн F Н,С —...
draw your cyclic model by adding the OH groups and H atoms to
figure below.
le the drawing a Unded black atom white atoms. Cl, use green For Br, use pe For all Lone chiral Cater b. Convert the open form of ribose into a eyelie form. Here's how: 1. Pull apart one of the Co bonds from the Catom, leaving the other end of the bond attached to the O atom. . Connect the free bond from the O...
2) Order the following alkenes from most stable to least stable Нас Нас с-сн, н,с Hас +C- Нас н CHs -CH3 H Hе most stable least stable (a) I (b) I (c) I ll (d) 7) Order the following C-H bonds from strongest to weakest. strongest weakest (a) (b) (c) II (d) 8) Which of the following is represents the lowest energy transition state for the addition of BH, to 2-methyl-1-propene? quCH «сHs нСи Нас (b) (a) Нив--н H H...
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