Draw molecules that satisfy the following prompts i-iii. All molecules must have 8-10 Carbon atoms AND...
Draw molecules that satisfy the following prompts i-iii.
All molecules must have 8-10 Carbon atoms AND exactly 2 Heteroatoms (i.e. atoms that are not carbon or hydrogen atoms). You may not use the same molecule twice for any parts of this question. You do not need to look up solubility information, but the answers must be reasonable. Also, the structures must be reasonable (improper structures, e.g. carbon with 5 bonds, or oxygen with one bond and no charge, will not receive any credit).
i) Draw two molecules that will be separated from each other if placed in a separatory funnel with dichloromethane and 2.5 M NaOH(aq).
ii) Draw two molecules that will be separated from each other if placed in a separatory funnel with 2.5 M HCl(aq) and dichloromethane.
iii) Draw two molecules thatwill NOT be separated from each other if placed in a separatory funnel with 2.5 M HCl(aq) and dichloromethane.
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Draw molecules that satisfy the following prompts i-iii.
All molecules must have 8-10 Carbon atoms AND...
Draw molecules that satisfy the following prompts i-iii. All molecules must have 8-10 Carbon atoms AND...
Draw molecules that satisfy the following prompts i-iii. All molecules must have 8-10 Carbon atoms AND exactly 2 Heteroatoms (i.e. atoms that are not carbon or hydrogen atoms). You may not use the same molecule twice for any parts of this question. You do not need to look up solubility information, but the answers must be reasonable. Also, the structures must be reasonable (improper structures, e.g. carbon with 5 bonds, or oxygen with one bond and no charge, will not...
6) Draw molecules that satisfy the following prompts i- i1i. All molecules must have a minimum...
6) Draw molecules that satisfy the following prompts i- i1i. All molecules must have a minimum of 13 Carbon atoms and exactly 2 heteroatoms (i.e. atoms that are not carbon or hydrogen atoms). You may not use the same molecule twice for any parts of this question. Structures must be drawn using ChemBioDraw. You do not need to look up solubility information, but the answers must be reasonable (supported by the concepts that we have discussed). Also, the structures must...
Two different molecules have the formula C2H2Cl2. Draw a Lewis structure for each molecule. (All the...
Two different molecules have the formula C2H2Cl2. Draw a Lewis structure for each molecule. (All the H and Cl atoms are bonded to carbon. The two carbon atoms are bonded to each other.)
14) Propose a multistep synthesis of the following compound. All carbon atoms in the product must...
14) Propose a multistep synthesis of the following compound. All carbon atoms in the product must come cyclohexene and from alkanes, alkenes, alkynes, and alkyl halides that contain 3 or fewer carbon atoms. You can use other reagents as necessary. You do not have to draw any curved- arrow mechanisms. While you do not have the products of each synthetic step or explain your synthetic logic, you are strongly encouraged to in order to be eligible for more partial credit....
Part B N2O Note that the arangement of the atoms is as follows: (N N O) Draw all the molecules by placing atoms on the...
Part B N2O Note that the arangement of the atoms is as follows: (N N O) Draw all the molecules by placing atoms on the grid and connecting them with bonds. Include all hydrogen atoms and all lone pairs of electrons. Include brackets for polyatomic ions. A double-headed arrow is not needed. LD C? s PFBra x oN More Request Answer Submit Draw two resonance structures for each of the following molecules or ions Part A H2 CNO2(with C and...
Week 10- Constitutional isomers Constitutional isomers have the same molecular formula, but their atoms are bonded...
Week 10- Constitutional isomers Constitutional isomers have the same molecular formula, but their atoms are bonded in different orders. These may be further distinguished as chain isomers, which differ only in hydrocarbon chain structure, positional isomers, which differ in the location of a functional group, and functional group isomers which differ in the nature of their functional groups. Typically chain and position isomers show only modest differences in their physical and chemical properties, while functional group isomers differ greatly from...
PART 2 Draw the most accurate 'H-NMR spectrum you can for the following molecules. Show all...
PART 2 Draw the most accurate 'H-NMR spectrum you can for the following molecules. Show all signals including an accurate representation of splitting, intensity and position. Assume no signal overlap (i.e. if you expect signals have similar chemical shifts, just place them next to each other). Clearly label the integration value for each signal. Indicate the correlation between each proton (HA, HB, etc) and each signal (label signals A, B, etc.) ppm 12.5 10 11 O ppm 12.5 10 ii...
3. Cyclic compounds The presence of the ring in all but very large ring cyclic molecules...
3. Cyclic compounds The presence of the ring in all but very large ring cyclic molecules prevents full rotation of the ring atoms. For this reason, stereoisomerism may also occur in cyclic molecules. a) Prepare a model of cyclohexane, C6H12. Draw the condensed formula. b) Build a model of methylcyclohexane (C7H14) by replacing one of the hydrogens of cyclohexane with a methyl group. Draw the skeletal formula for methylcyclohexane. 2 c) How many different isomers exist for methylcyclohexane (CyH34)? d)...
A. Enantiomers: Certain substances have the unique property of rotating the plane of plane-polarized light. Such...
A. Enantiomers: Certain substances have the unique property of rotating the plane of plane-polarized light. Such light rotation is detectable with the aid of a polarimeter. In order for a molecule to be optically active it must be chiral. Chiral objects lack a plane of symmetry and are non-superimposable on their mirror images. A sp?- hybridized carbon atom can fulfill these requirements if all four of its substituents are different. 1. Methane a) Prepare a methane molecule and then substitute...
Construct a flow chart describing the seperation of the mixture and the isolation of each compound...
Construct a flow chart describing the seperation of the
mixture and the isolation of each compound in this experiment. (Lab
steps/procedures includes for reference)
4. Construct a flow chart describing the separation of the mixture and the isolation of each compound in this experiment. A commonly used method of separating a mixture of organic compounds is known as liquid-liquid extraction. Most reactions of organic compounds require extraction at some stage of product purification. In this experiment you will use extraction...
6) Draw molecules that satisfy the following prompts i- i1i. All molecules must have a minimum of 13 Carbon atoms and exactly 2 heteroatoms (i.e. atoms that are not carbon or hydrogen atoms). You may not use the same molecule twice for any parts of this question. Structures must be drawn using ChemBioDraw. You do not need to look up solubility information, but the answers must be reasonable (supported by the concepts that we have discussed). Also, the structures must...
14) Propose a multistep synthesis of the following compound. All carbon atoms in the product must come cyclohexene and from alkanes, alkenes, alkynes, and alkyl halides that contain 3 or fewer carbon atoms. You can use other reagents as necessary. You do not have to draw any curved- arrow mechanisms. While you do not have the products of each synthetic step or explain your synthetic logic, you are strongly encouraged to in order to be eligible for more partial credit....
Part B N2O Note that the arangement of the atoms is as follows: (N N O) Draw all the molecules by placing atoms on the grid and connecting them with bonds. Include all hydrogen atoms and all lone pairs of electrons. Include brackets for polyatomic ions. A double-headed arrow is not needed. LD C? s PFBra x oN More Request Answer Submit Draw two resonance structures for each of the following molecules or ions Part A H2 CNO2(with C and...
Week 10- Constitutional isomers Constitutional isomers have the same molecular formula, but their atoms are bonded in different orders. These may be further distinguished as chain isomers, which differ only in hydrocarbon chain structure, positional isomers, which differ in the location of a functional group, and functional group isomers which differ in the nature of their functional groups. Typically chain and position isomers show only modest differences in their physical and chemical properties, while functional group isomers differ greatly from...
PART 2 Draw the most accurate 'H-NMR spectrum you can for the following molecules. Show all signals including an accurate representation of splitting, intensity and position. Assume no signal overlap (i.e. if you expect signals have similar chemical shifts, just place them next to each other). Clearly label the integration value for each signal. Indicate the correlation between each proton (HA, HB, etc) and each signal (label signals A, B, etc.) ppm 12.5 10 11 O ppm 12.5 10 ii...
3. Cyclic compounds The presence of the ring in all but very large ring cyclic molecules prevents full rotation of the ring atoms. For this reason, stereoisomerism may also occur in cyclic molecules. a) Prepare a model of cyclohexane, C6H12. Draw the condensed formula. b) Build a model of methylcyclohexane (C7H14) by replacing one of the hydrogens of cyclohexane with a methyl group. Draw the skeletal formula for methylcyclohexane. 2 c) How many different isomers exist for methylcyclohexane (CyH34)? d)...
A. Enantiomers: Certain substances have the unique property of rotating the plane of plane-polarized light. Such light rotation is detectable with the aid of a polarimeter. In order for a molecule to be optically active it must be chiral. Chiral objects lack a plane of symmetry and are non-superimposable on their mirror images. A sp?- hybridized carbon atom can fulfill these requirements if all four of its substituents are different. 1. Methane a) Prepare a methane molecule and then substitute...
Construct a flow chart describing the seperation of the
mixture and the isolation of each compound in this experiment. (Lab
steps/procedures includes for reference)
4. Construct a flow chart describing the separation of the mixture and the isolation of each compound in this experiment. A commonly used method of separating a mixture of organic compounds is known as liquid-liquid extraction. Most reactions of organic compounds require extraction at some stage of product purification. In this experiment you will use extraction...
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