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Shit Alt 4. (4 pts.) The mechanism for the...
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...
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...
Question 2: Determine in the following examples if the base is strong enough to deprotonate the...
Question 2: Determine in the following examples if the base is strong enough to deprotonate the terminal alkyne. сH, нс. t-BuOK + Cн Question 3: A terminal alkyne is prepared by treating the dihalide with excess (xs) sodium amide, followed by water. Predict the major product and draw a mechanism for its formation: Br 1) xs NaNHNH 2) Hо Br Identify reagents that you could use to achieve the following transformations: CH3 Нас Н,с CH3 CH3 HyC Н.с CHs CH3...
1. Draw the following compounds. Each question is out of two marks. Drawing Name 2-phenyl hexanal...
1. Draw the following compounds. Each question is out of two marks. Drawing Name 2-phenyl hexanal 2-ethyl octan-1,2,7-triol para-chlorophenol cis-pent-3-en-2-ol 1,3-diphenylpropan-2-one ethyl butanoate 4-hydroxy-4-propyl hept-2,5-diene-1-amide N-pentyl-2,3-difluoro butanamide 2. Name the following compounds. Each question is out of two marks. Drawing Name CH3 CH Н.С Он Н. Н. Н.С Н. Н Н.С Н Н с Н CH CH НАС Н.С. CH2 Н.С. Н сн. HC H2 CH, CH Он Н.С CH, Н С. Н H C Н.С Н. На CH Н.С...
4. Alcohols undergo two major types of elimination reactions. Classify the following reactions as DEHYDRATION (removal...
4. Alcohols undergo two major types of elimination reactions. Classify the following reactions as DEHYDRATION (removal of W U RCACIAD 20s Sax oa or DEHYDROGENATION (removal of hydrogen). ater) а. НС, CH2 concentrated., acid CH2 Cн Hас CH2 A-CH2 CH CH2 Н,с сн CH3 CH3 OH (Oil-D b. Н,С CH CH2 O CH2 CH2 CH H3C CHh CHh CH CH CH2 Н.С CH3 CH3 ОН CH CH2 CH2 CH2 CH2 C. CH, CH, "oн Но
4. Alcohols undergo two major...
alexis Naming Hydrocarbons Compatibility Mode Review View Help Mailings References Layout 1 I 2 3 Naming...
alexis Naming Hydrocarbons Compatibility Mode Review View Help Mailings References Layout 1 I 2 3 Naming Worksheet - Hydrocarbons Name: Name of compound H,с- CH CH сH, 1 CH2 CH3 Нас Сн CH 2. Нас нас Methylcyclohexane 3. CHз I Br 4. Hас-нс -сн>-CH-CH, Н.с -сн CH3 -CHз 5. Н.с — сн — с CH3 H3C-CH-CHECH-CH2 CH3 6 но 7. Нс с сн 8 DFocus он DELL O co 6 1 Нас - CH2 CH3 C-CH3 CH3 H3C-CH2-CHECH-CH2 CH3 5....
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...
help with all of these ! Question 8: Which is the better retrosynthesis for the given target molecule? Explain and...
help with all of these !
Question 8: Which is the better retrosynthesis for the given target molecule? Explain and provide a one-step synthesis of the target molecule. Br Br Hас Hас Hас .CH3 b) NaQH CHy Question 7: Draw the plausible mechanism for each of the folllowing transformations: a) CHy Не нс CHs CH СH, CH3 conc. H,SO -CH3 heat CH он Question 5 Predict the major and minor products for the following reactions: a) NaSH Н,с b) Br...
ЕОC Problem 11.030 a. Draw the products formed when the triglyceride is saponified. Enter your answers from largest mas...
ЕОC Problem 11.030 a. Draw the products formed when the triglyceride is saponified. Enter your answers from largest mass to smallest mass. сH,(CH,),СH-CHCH), С -осн, CH2(CH)12 C OCH II CH,(CH), CH-CHCH,), С- -осн, Your answer is partially correct. Try again нс Na Edit Product 1 (largest molecular mass product) НаС Na Edit Product 2 O O O=O Edit Na Н,с. Product 3 -OH -Он Edit -OH Product 4 (smallest molecular mass product) Choose the drawings of a trans fat that...
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...
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...
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...
Question 2: Determine in the following examples if the base is strong enough to deprotonate the terminal alkyne. сH, нс. t-BuOK + Cн Question 3: A terminal alkyne is prepared by treating the dihalide with excess (xs) sodium amide, followed by water. Predict the major product and draw a mechanism for its formation: Br 1) xs NaNHNH 2) Hо Br Identify reagents that you could use to achieve the following transformations: CH3 Нас Н,с CH3 CH3 HyC Н.с CHs CH3...
1. Draw the following compounds. Each question is out of two marks. Drawing Name 2-phenyl hexanal 2-ethyl octan-1,2,7-triol para-chlorophenol cis-pent-3-en-2-ol 1,3-diphenylpropan-2-one ethyl butanoate 4-hydroxy-4-propyl hept-2,5-diene-1-amide N-pentyl-2,3-difluoro butanamide 2. Name the following compounds. Each question is out of two marks. Drawing Name CH3 CH Н.С Он Н. Н. Н.С Н. Н Н.С Н Н с Н CH CH НАС Н.С. CH2 Н.С. Н сн. HC H2 CH, CH Он Н.С CH, Н С. Н H C Н.С Н. На CH Н.С...
4. Alcohols undergo two major types of elimination reactions. Classify the following reactions as DEHYDRATION (removal of W U RCACIAD 20s Sax oa or DEHYDROGENATION (removal of hydrogen). ater) а. НС, CH2 concentrated., acid CH2 Cн Hас CH2 A-CH2 CH CH2 Н,с сн CH3 CH3 OH (Oil-D b. Н,С CH CH2 O CH2 CH2 CH H3C CHh CHh CH CH CH2 Н.С CH3 CH3 ОН CH CH2 CH2 CH2 CH2 C. CH, CH, "oн Но
4. Alcohols undergo two major...
alexis Naming Hydrocarbons Compatibility Mode Review View Help Mailings References Layout 1 I 2 3 Naming Worksheet - Hydrocarbons Name: Name of compound H,с- CH CH сH, 1 CH2 CH3 Нас Сн CH 2. Нас нас Methylcyclohexane 3. CHз I Br 4. Hас-нс -сн>-CH-CH, Н.с -сн CH3 -CHз 5. Н.с — сн — с CH3 H3C-CH-CHECH-CH2 CH3 6 но 7. Нс с сн 8 DFocus он DELL O co 6 1 Нас - CH2 CH3 C-CH3 CH3 H3C-CH2-CHECH-CH2 CH3 5....
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...
help with all of these !
Question 8: Which is the better retrosynthesis for the given target molecule? Explain and provide a one-step synthesis of the target molecule. Br Br Hас Hас Hас .CH3 b) NaQH CHy Question 7: Draw the plausible mechanism for each of the folllowing transformations: a) CHy Не нс CHs CH СH, CH3 conc. H,SO -CH3 heat CH он Question 5 Predict the major and minor products for the following reactions: a) NaSH Н,с b) Br...
ЕОC Problem 11.030 a. Draw the products formed when the triglyceride is saponified. Enter your answers from largest mass to smallest mass. сH,(CH,),СH-CHCH), С -осн, CH2(CH)12 C OCH II CH,(CH), CH-CHCH,), С- -осн, Your answer is partially correct. Try again нс Na Edit Product 1 (largest molecular mass product) НаС Na Edit Product 2 O O O=O Edit Na Н,с. Product 3 -OH -Он Edit -OH Product 4 (smallest molecular mass product) Choose the drawings of a trans fat that...
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...
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