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(b) How many t bonds in 7. In each case, circle the molecule of the pair...
11). (12 pts) For each pair of nucleophiles, CIRCLE the one that is more nucleophilic, and...
11). (12 pts) For each pair of nucleophiles, CIRCLE the one that is more nucleophilic, and provide a short explanation for your choice. A) CH.CH.CH OH and CH CH CH NH B) CH-OH and C H-O"Nat C) I and Br" D) (CH-CH2),P (Triethylphosphine) and (CH-CH2),N (triethylamine)
7). a). Is the acetone molecule non-polar or polar? Circle. Non-polar Polar b). Sketch pictures of...
7). a). Is the acetone molecule non-polar or polar? Circle. Non-polar Polar b). Sketch pictures of the intermolecular forces that would occur between the molecules of acetone and the molecules of 2- propanone if you have a mixture of the two liquids. What would be the main type of IMF that is responsible for the attraction? (Give a name for the IMF). c). The pentane molecule and the 2-pentanone molecule both have five carbon atoms on their structures. Why 2-pentanone...
3. a) Draw both chair conformations for the molecule shown below. (2pts) b) Circle the most...
3. a) Draw both chair conformations for the molecule shown
below. (2pts) b) Circle the most stable conformation above. Give a
brief explanation on why your choice is more stable. (2pts)
b) Circle the most stable conformation above. Give a brief
explanation on why your choice is more stable. (2pts)
3. a) Draw both chair conformations for the molecule shown below. (2pts) HO OH b) Circle the most stable conformation above. Give a brief explanation on why your choice is...
1. For each pair, circle the molecule with the lower pK and provide a brief explanation...
1. For each pair, circle the molecule with the lower pK and provide a brief explanation for your choice. wale wabon ---- 2. For each molecule, draw the two possible chair conformers and circle the preferred conformer. a) cis-1,3-dimethylcyclohexane trans-1,4-dimethylcyclohexane 3. Draw all distinct isomers of dimethylcyclopropane and show the relationship as enantiomer, diastereomer or meso. 4. In each of the following pairs of compounds one is chiral and the other achiral, Circle the chiral compound in each. a) CH,CHCH=CH...
9. Draw all of the possible hydrogen bonds between the following molecule and water molecules. Indicate...
9. Draw all of the possible hydrogen bonds between the following molecule and water molecules. Indicate the hydrogen bonds with dotted lines. :N-CEN: H 10. Polar molecules can contain more than one type of attractive force. Fill in the following table answering the question "Is this attractive force present between molecules of the given compound?" Write yes or no for each force. Molecule Ionic Attraction H-Bond Dipole-Dipole London CHCl3 CH3OH NH2 65- *NH3-C-COO 11. For each of the following pairs...
он нас A CH3 B CHa 11) Match the molecule wi acetal 12) Circle the th...
он нас A CH3 B CHa 11) Match the molecule wi acetal 12) Circle the th the functional group _hemiacetal _ketal compound that has the higher boiling point and state a reason why -diethyl ether or 1-butanol N,N-dimethylethanamine or 1-butanamine 3-hexanol or 3-butanol - Butanamide or N-methyl-1-propanamide 13) Circle the compound that is more soluble in water and state a reason why -2-hexanol or 1-propanol N,N-dimethylpropanamide or pentanamide 1-butanol or diethyl ether -3- heptanamine or 3-pentanamine Glucose но. 6 HO-C-H...
Name Worksheet Alcohols, Aldehydes, Ketons 1. Circle the molecule which will have the highest boiling point:...
Name Worksheet Alcohols, Aldehydes, Ketons 1. Circle the molecule which will have the highest boiling point: CH,CH2CH3 CH2=CHCH, CH,CH2-OH 2. Classify these alcohols as 1º,2º, or 30: OH CH3CH2CHCHCH2CH2-OH: C1 CH) 4-choloro 3-hexene HH OHH H-C-C-C-C-H Η Η H H-C-H CH3CHCH OH 2-propanol H 3. Name each of these alcohols: CH,CH2CHCHCH2CH2-OH CH CH3CH2-OH Ethyl alcohol HH OHH H-C-C-C--H Η Η H H-CH CH,CHCH OH H Aldehydes and Ketons nonsolo 4. Give the IUPAC names for the following aldehydes: OH O...
Discussion Questions The structures of acetanilide and malonic acid are provided below 1. For each structure,...
Discussion Questions The structures of acetanilide and malonic acid are provided below 1. For each structure, draw circles around the polar and nonpolar regions of the molecule, and label each circled regiorn with the type of intermolecular attractive force it can use to interact with other molecules. Acetanilide Malonic Acid но CH2 OH 2. Now-thoroughly explain (on the basis of polarity/nonpolarity and intermolecular attractive forces) how the acetanilide was separated from the malonic acid by recrystallization from water. And explain...
9. (20pts) For each pair of molecules, circle the one with the indicated property: a) the...
9. (20pts) For each pair of molecules, circle the one with the indicated property: a) the better nucleophile in MeCN b) the better nucleophile in CH3OH CH3S or CH30 c) the ion that will give the higher substitution to elimination product ratio CH3S or CH30 Won d) the more reactive alkyl halide in a solvolysis reaction aior e) the more reactive alcohol towards substitution — он оr f) the more reactive alkyl halide in an E2 reaction balt Br g)...
10. Which of the following roduct, if any, is not a heterocyclic amine? CHE HCNN Ho all of them are heterocy...
10. Which of the following roduct, if any, is not a heterocyclic amine? CHE HCNN Ho all of them are heterocyclic amines i Cho OH HOH OH LCH, HOW N & CH₂ IN-CH HO (e) (b) 11. What is the IUPAC har is the IUPAC name of the following compound pound? OOH 9 TOH OH 9 hydroxy-1.4-dimethyl-5-oxohexanoic acid hydroxy-2-methyl-5-oxohexanoic acid (d) 2-hydro ydroxy-2,5-dimethyl-6-oxoheptanoic acid 2-hydroxy-1-methyl-4-oxopentanoic acid (e) 3-hydrox 3-hydroxy-2,5-dimethyl-5-oxohexanoic acid O 3-hydroxy-2,5-dimethy 12. Predict the product/s, the product/s, if any,...
11). (12 pts) For each pair of nucleophiles, CIRCLE the one that is more nucleophilic, and provide a short explanation for your choice. A) CH.CH.CH OH and CH CH CH NH B) CH-OH and C H-O"Nat C) I and Br" D) (CH-CH2),P (Triethylphosphine) and (CH-CH2),N (triethylamine)
7). a). Is the acetone molecule non-polar or polar? Circle. Non-polar Polar b). Sketch pictures of the intermolecular forces that would occur between the molecules of acetone and the molecules of 2- propanone if you have a mixture of the two liquids. What would be the main type of IMF that is responsible for the attraction? (Give a name for the IMF). c). The pentane molecule and the 2-pentanone molecule both have five carbon atoms on their structures. Why 2-pentanone...
3. a) Draw both chair conformations for the molecule shown
below. (2pts) b) Circle the most stable conformation above. Give a
brief explanation on why your choice is more stable. (2pts)
b) Circle the most stable conformation above. Give a brief
explanation on why your choice is more stable. (2pts)
3. a) Draw both chair conformations for the molecule shown below. (2pts) HO OH b) Circle the most stable conformation above. Give a brief explanation on why your choice is...
1. For each pair, circle the molecule with the lower pK and provide a brief explanation for your choice. wale wabon ---- 2. For each molecule, draw the two possible chair conformers and circle the preferred conformer. a) cis-1,3-dimethylcyclohexane trans-1,4-dimethylcyclohexane 3. Draw all distinct isomers of dimethylcyclopropane and show the relationship as enantiomer, diastereomer or meso. 4. In each of the following pairs of compounds one is chiral and the other achiral, Circle the chiral compound in each. a) CH,CHCH=CH...
9. Draw all of the possible hydrogen bonds between the following molecule and water molecules. Indicate the hydrogen bonds with dotted lines. :N-CEN: H 10. Polar molecules can contain more than one type of attractive force. Fill in the following table answering the question "Is this attractive force present between molecules of the given compound?" Write yes or no for each force. Molecule Ionic Attraction H-Bond Dipole-Dipole London CHCl3 CH3OH NH2 65- *NH3-C-COO 11. For each of the following pairs...
он нас A CH3 B CHa 11) Match the molecule wi acetal 12) Circle the th the functional group _hemiacetal _ketal compound that has the higher boiling point and state a reason why -diethyl ether or 1-butanol N,N-dimethylethanamine or 1-butanamine 3-hexanol or 3-butanol - Butanamide or N-methyl-1-propanamide 13) Circle the compound that is more soluble in water and state a reason why -2-hexanol or 1-propanol N,N-dimethylpropanamide or pentanamide 1-butanol or diethyl ether -3- heptanamine or 3-pentanamine Glucose но. 6 HO-C-H...
Name Worksheet Alcohols, Aldehydes, Ketons 1. Circle the molecule which will have the highest boiling point: CH,CH2CH3 CH2=CHCH, CH,CH2-OH 2. Classify these alcohols as 1º,2º, or 30: OH CH3CH2CHCHCH2CH2-OH: C1 CH) 4-choloro 3-hexene HH OHH H-C-C-C-C-H Η Η H H-C-H CH3CHCH OH 2-propanol H 3. Name each of these alcohols: CH,CH2CHCHCH2CH2-OH CH CH3CH2-OH Ethyl alcohol HH OHH H-C-C-C--H Η Η H H-CH CH,CHCH OH H Aldehydes and Ketons nonsolo 4. Give the IUPAC names for the following aldehydes: OH O...
Discussion Questions The structures of acetanilide and malonic acid are provided below 1. For each structure, draw circles around the polar and nonpolar regions of the molecule, and label each circled regiorn with the type of intermolecular attractive force it can use to interact with other molecules. Acetanilide Malonic Acid но CH2 OH 2. Now-thoroughly explain (on the basis of polarity/nonpolarity and intermolecular attractive forces) how the acetanilide was separated from the malonic acid by recrystallization from water. And explain...
9. (20pts) For each pair of molecules, circle the one with the indicated property: a) the better nucleophile in MeCN b) the better nucleophile in CH3OH CH3S or CH30 c) the ion that will give the higher substitution to elimination product ratio CH3S or CH30 Won d) the more reactive alkyl halide in a solvolysis reaction aior e) the more reactive alcohol towards substitution — он оr f) the more reactive alkyl halide in an E2 reaction balt Br g)...
10. Which of the following roduct, if any, is not a heterocyclic amine? CHE HCNN Ho all of them are heterocyclic amines i Cho OH HOH OH LCH, HOW N & CH₂ IN-CH HO (e) (b) 11. What is the IUPAC har is the IUPAC name of the following compound pound? OOH 9 TOH OH 9 hydroxy-1.4-dimethyl-5-oxohexanoic acid hydroxy-2-methyl-5-oxohexanoic acid (d) 2-hydro ydroxy-2,5-dimethyl-6-oxoheptanoic acid 2-hydroxy-1-methyl-4-oxopentanoic acid (e) 3-hydrox 3-hydroxy-2,5-dimethyl-5-oxohexanoic acid O 3-hydroxy-2,5-dimethy 12. Predict the product/s, the product/s, if any,...
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