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3. The following molecule has carbon alumns in total and is an example of a (saturated...
1. Draw the following molecules using line structures. (20 points) (L.)4-methyl-1-pentene (2.) -1,2-dimethyl-cyclop...
1. Draw the following molecules using line structures. (20 points) (L.)4-methyl-1-pentene (2.) -1,2-dimethyl-cycloptutade 2. Determine the molecular formula for the following structurw. (20points) 3. The following molecule bes c arbon atoms in total and is an example of a (saturaledunsaturated fatty acid with _ſcis/trans) configuration. (15 points) 4. Draw the mirror Image of the following molecule. Then, determine if they are enantiomers or identical. Circle the chiral center if prosent (15 points) CHE 5. Circle and label the carboxylic acid...
5) (3 pts) Draw an essential -6 fatty acid with 18 carbons and two cis double bonds. Number carbon atoms in this fa...
5) (3 pts) Draw an essential -6 fatty acid with 18 carbons and two cis double bonds. Number carbon atoms in this fatty acid starting at the carboxyl group. 6) (3 pts) Draw an essential 0-3 fatty acid with 18 carbons and three cis-double bonds. Number carbon atoms in this fatty acid starting at the carboxyl group. 7) (3 pts) Draw an unnatural trans-fatty acid arising from partial hydrogenation that contains 14 carbons and two double bonds, one of which...
3) (6 pts) Draw a line structure of an organic molecule that contains exactly 12 carbons,...
3) (6 pts) Draw a line structure of an organic molecule that contains exactly 12 carbons, five-membered ring an nitrogen atom, an ester group and a secondary alcohol group. Number all carbon atoms. Place an asterisk (*) next to any chiral carbons that may exist in the structure and state how many stereoisomers are possible for the molecule. # of chiral carbons: # of possible stereoisomers: 4) (6 pts) Draw a line structure of an organic molecule that contains 12...
3. Diastereomers and Meso Forms. When a molecule has two or more stereogenic centers, stereoisomers that...
3. Diastereomers and Meso Forms. When a molecule has two or more stereogenic centers, stereoisomers that are not mirror images can exist; these are called diastereoisomers. Within this general class, there are special types of stereoisomers that are always optically inactive and are called meso forms. Construct a model with four different colored balls about a carbon center. Construct another identical to the first and verify this by the superimposition test. Now remove the same colored balls, blue (C from...
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...
1. In each molecule A-F below, circle and name two functional groups/moieties present in the molecule....
1. In each molecule A-F below, circle and name two functional groups/moieties present in the molecule. Select from the list provided. [alcohol, ether, aldehyde, carboxylic acid, ester, amine, amide, propyl, alkyne, alkene - label as cis or trans when applicable, arene (for aromatic group)]. H2N- CH-OH CH2 HO H2CO | 0 NHA H2N IZ HO I- 0 m
please solve all the questions 5. Label the chiral carbon(s) in each of the following structures...
please solve all the questions
5. Label the chiral carbon(s) in each of the following structures with an asterisk (*). H OHH OH H-C-C=C – H | H H OH 6. Use your knowledge of the Cahn-Ingold-Prelog sequence rules to rank the substituents in order of priority, highest priority first: HO HO The alcohol The chlorine The ethyl group The carboxylic acid group 7. Identify the following as chiral or achiral. If chiral, identify the chiral carbon(s) with an asterik...
#1 please answer all components. Question 1 (6 points) Consider the following fatty acids. Label each one as saturated, monounsaturated, polyunsaturated, or trans. Circle the one you would expect...
#1
please answer all components.
Question 1 (6 points) Consider the following fatty acids. Label each one as saturated, monounsaturated, polyunsaturated, or trans. Circle the one you would expect to have the lowest melting point. Draw a rectangle around the one you would expect to be the most resistant to oxidation но но но HO
Question 1 (6 points) Consider the following fatty acids. Label each one as saturated, monounsaturated, polyunsaturated, or trans. Circle the one you would expect to...
draw an example of a molecule containing the functional groups give the systematic name what is...
draw an example of a molecule containing the functional groups
give the systematic name
what is its major mode of interaction with other molecules
(hint: 3 forces)
help please... im lost. thanks in advance.
1. Aldehyde 2. Ketone 3. Amine 4. Amide 5. Alcohol 6. Ether 7. Carboxylic acid 8. Ester (of carboxylic acid) 9. cis-Alkene 10. trans-Alkene
super easy points Aldehydes and Ketones Classify each molecule as an aldehyde, ketone, or neither. Drag...
super easy points
Aldehydes and Ketones Classify each molecule as an aldehyde, ketone, or neither. Drag the appropriate molecules to their respective bins. Draw the aldehyde produced from the oxidation of CH3CH2CH2C(CH3)2CH2OH. Draw the molecule by placing atoms on the grid and connecting them with bonds. Include all hydrogen atoms. Draw the ketone produced from the oxidation of 2-pentanol. Draw the molecule by placing atoms on the grid and connecting them with bonds. Include all hydrogen atoms. Carboxylic Acids and...
1. Draw the following molecules using line structures. (20 points) (L.)4-methyl-1-pentene (2.) -1,2-dimethyl-cycloptutade 2. Determine the molecular formula for the following structurw. (20points) 3. The following molecule bes c arbon atoms in total and is an example of a (saturaledunsaturated fatty acid with _ſcis/trans) configuration. (15 points) 4. Draw the mirror Image of the following molecule. Then, determine if they are enantiomers or identical. Circle the chiral center if prosent (15 points) CHE 5. Circle and label the carboxylic acid...
5) (3 pts) Draw an essential -6 fatty acid with 18 carbons and two cis double bonds. Number carbon atoms in this fatty acid starting at the carboxyl group. 6) (3 pts) Draw an essential 0-3 fatty acid with 18 carbons and three cis-double bonds. Number carbon atoms in this fatty acid starting at the carboxyl group. 7) (3 pts) Draw an unnatural trans-fatty acid arising from partial hydrogenation that contains 14 carbons and two double bonds, one of which...
3) (6 pts) Draw a line structure of an organic molecule that contains exactly 12 carbons, five-membered ring an nitrogen atom, an ester group and a secondary alcohol group. Number all carbon atoms. Place an asterisk (*) next to any chiral carbons that may exist in the structure and state how many stereoisomers are possible for the molecule. # of chiral carbons: # of possible stereoisomers: 4) (6 pts) Draw a line structure of an organic molecule that contains 12...
3. Diastereomers and Meso Forms. When a molecule has two or more stereogenic centers, stereoisomers that are not mirror images can exist; these are called diastereoisomers. Within this general class, there are special types of stereoisomers that are always optically inactive and are called meso forms. Construct a model with four different colored balls about a carbon center. Construct another identical to the first and verify this by the superimposition test. Now remove the same colored balls, blue (C from...
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...
1. In each molecule A-F below, circle and name two functional groups/moieties present in the molecule. Select from the list provided. [alcohol, ether, aldehyde, carboxylic acid, ester, amine, amide, propyl, alkyne, alkene - label as cis or trans when applicable, arene (for aromatic group)]. H2N- CH-OH CH2 HO H2CO | 0 NHA H2N IZ HO I- 0 m
please solve all the questions
5. Label the chiral carbon(s) in each of the following structures with an asterisk (*). H OHH OH H-C-C=C – H | H H OH 6. Use your knowledge of the Cahn-Ingold-Prelog sequence rules to rank the substituents in order of priority, highest priority first: HO HO The alcohol The chlorine The ethyl group The carboxylic acid group 7. Identify the following as chiral or achiral. If chiral, identify the chiral carbon(s) with an asterik...
#1
please answer all components.
Question 1 (6 points) Consider the following fatty acids. Label each one as saturated, monounsaturated, polyunsaturated, or trans. Circle the one you would expect to have the lowest melting point. Draw a rectangle around the one you would expect to be the most resistant to oxidation но но но HO
Question 1 (6 points) Consider the following fatty acids. Label each one as saturated, monounsaturated, polyunsaturated, or trans. Circle the one you would expect to...
draw an example of a molecule containing the functional groups
give the systematic name
what is its major mode of interaction with other molecules
(hint: 3 forces)
help please... im lost. thanks in advance.
1. Aldehyde 2. Ketone 3. Amine 4. Amide 5. Alcohol 6. Ether 7. Carboxylic acid 8. Ester (of carboxylic acid) 9. cis-Alkene 10. trans-Alkene
super easy points
Aldehydes and Ketones Classify each molecule as an aldehyde, ketone, or neither. Drag the appropriate molecules to their respective bins. Draw the aldehyde produced from the oxidation of CH3CH2CH2C(CH3)2CH2OH. Draw the molecule by placing atoms on the grid and connecting them with bonds. Include all hydrogen atoms. Draw the ketone produced from the oxidation of 2-pentanol. Draw the molecule by placing atoms on the grid and connecting them with bonds. Include all hydrogen atoms. Carboxylic Acids and...
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