names of the compounds 2. Which of the compounds you built are structural isomers? Include the n and explain your choices. (4 marks) 3. Which of these compounds would have the highest solubility? Explain. (2 marks) 4. Select three of the molecules you have created above. Then draw and name a structural isomer that would still belong to the same organic family as the original molecule. (3 marks) 5. Do any of the molecules you have drawn have a stereoisomer ? Explain. (2 marks)
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Using the information from the chart answer the following questions in full sentences.
help with these questions, I need clear explanations to understand 24. Name the following compounds. (6...
help with these questions, I
need clear explanations to understand
24. Name the following compounds. (6 marks total) a) Br Br Br c= c CH3 Br b) CH3-CH2-CH-CH2-OH OH 0 CH3-CH-C-CH2-CH2-F CH3 25. 26. Draw the structural formula for the following compounds. (6 marks total) a) 4,4-dichloropentanal b) 2-methylbutanol c) 3,3-dichlorohexane Draw and name all of the structural isomers that are ketones with five carbon atoms in its longest chain and the molecular formula C H, O. Can this molecular...
I need help with the answers but also with the explanation and how to get there Draw and name all of the structural isom...
I need help with the answers but
also with the explanation and how to get there
Draw and name all of the structural isomers that are ketones with five carbon atoms in 26. its longest chain and the molecular formula CHO. Can this molecular formula also have an aldehyde structure? If so, illustrate and name the aldehyde. Can this be drawn as an ether? Explain. (6 marks) Write chemical equations for the synthesis of 2-pentanol from an alkene. Use structural...
POSTLAB QUESTIONS Name Date Instructor Organic Models and Nomenclature 1. Name the following compounds using the...
POSTLAB QUESTIONS Name Date Instructor Organic Models and Nomenclature 1. Name the following compounds using the IUPAC nomenclature system: a. CH CH.CH,CH,CH, Peptone b. CH CH CHCHCH, I methu Pentare CH, CH, c. CH CH CCH CH 2. Draw the constitutional (structural) isomers of C,H, 3. Draw the structure of trans-2-butene, and then sketch the product that would result if this compound reacted with bromine, Br, Postlab Questions: Organic Models and Nomencla 4. Circle the functional groups on the molecules...
If i could get some help on either of these 2 worksheets i would greatly appreciate...
If i could get some help on either of these 2 worksheets i
would greatly appreciate it! Thanks so mich!
do some molecules with the same formula (or even connectivity!) have different properties? ACQUIRE (USING MODELS!) 1. Fill in the following tables and BUILD each structure as you go. Have your instructor check your answers after each table or as directed Name and Condensed structure Skeletal structure Molecular formula Name: C8H18 2,3-dimethylhexane Molecular formula: C&HI8 Constitutional (structural) isomer of A...
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...
Answer the following questions using these molecules: diethyl ether, chloroacetone, methyl ethyl ketone, xylene, 2-butene, 2,2-dimethyl...
Answer the following questions using these molecules: diethyl ether, chloroacetone, methyl ethyl ketone, xylene, 2-butene, 2,2-dimethyl propane, acetic acid a) Which compounds would show only singlets in the proton spectrum, in the region of chemical shift less than/equal to 6? b) Which methyl group among all the compounds will give a proton signal at highest field? c) Which compound(s) will give a proton shift at lowest field? d) Which compound(s) will give a carbon signal at lowest field? e) Which...
4-chloro-3, 4-dimethylnonan-1-amine Assignment 3: Chiral Carbons and Stereoisomers On a page titled Chiral Carbons...
4-chloro-3, 4-dimethylnonan-1-amine
Assignment 3: Chiral Carbons and Stereoisomers On a page titled Chiral Carbons draw using a chemical drawing program or other computer generated form the expanded structure of your molecule. No hand drawn structures will be accepted. O Determine if your molecule contains any chiral carbons. If there are chiral carbons in your molecule, circle or highlight all of them. If your molecule does not contain any chiral carbons explain why none of the carbons are chiral. One a...
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...
2-methylocta-4,6-dien-1-amine Assignment 1: Draw your molecule from IUPAC name
2-methylocta-4,6-dien-1-amineAssignment 1: Draw your molecule from IUPAC
name Using the given IUPAC name, draw your molecule Complete the cover page (p.1) of your portfolio with the
following:o Structural formula of the moleculeo IUPAC name Use a thin, clear binder or report cover to protect the
portfolio Submit the following in the binder:o Cover page as described above (page 1)Assignment 2: Formula, Molar Mass and Functional
Groups On a page titled Expanded Structural Formula draw the expanded
structure of themolecule.o Show...
help with these questions, I
need clear explanations to understand
24. Name the following compounds. (6 marks total) a) Br Br Br c= c CH3 Br b) CH3-CH2-CH-CH2-OH OH 0 CH3-CH-C-CH2-CH2-F CH3 25. 26. Draw the structural formula for the following compounds. (6 marks total) a) 4,4-dichloropentanal b) 2-methylbutanol c) 3,3-dichlorohexane Draw and name all of the structural isomers that are ketones with five carbon atoms in its longest chain and the molecular formula C H, O. Can this molecular...
I need help with the answers but
also with the explanation and how to get there
Draw and name all of the structural isomers that are ketones with five carbon atoms in 26. its longest chain and the molecular formula CHO. Can this molecular formula also have an aldehyde structure? If so, illustrate and name the aldehyde. Can this be drawn as an ether? Explain. (6 marks) Write chemical equations for the synthesis of 2-pentanol from an alkene. Use structural...
POSTLAB QUESTIONS Name Date Instructor Organic Models and Nomenclature 1. Name the following compounds using the IUPAC nomenclature system: a. CH CH.CH,CH,CH, Peptone b. CH CH CHCHCH, I methu Pentare CH, CH, c. CH CH CCH CH 2. Draw the constitutional (structural) isomers of C,H, 3. Draw the structure of trans-2-butene, and then sketch the product that would result if this compound reacted with bromine, Br, Postlab Questions: Organic Models and Nomencla 4. Circle the functional groups on the molecules...
If i could get some help on either of these 2 worksheets i
would greatly appreciate it! Thanks so mich!
do some molecules with the same formula (or even connectivity!) have different properties? ACQUIRE (USING MODELS!) 1. Fill in the following tables and BUILD each structure as you go. Have your instructor check your answers after each table or as directed Name and Condensed structure Skeletal structure Molecular formula Name: C8H18 2,3-dimethylhexane Molecular formula: C&HI8 Constitutional (structural) isomer of A...
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...
4-chloro-3, 4-dimethylnonan-1-amine
Assignment 3: Chiral Carbons and Stereoisomers On a page titled Chiral Carbons draw using a chemical drawing program or other computer generated form the expanded structure of your molecule. No hand drawn structures will be accepted. O Determine if your molecule contains any chiral carbons. If there are chiral carbons in your molecule, circle or highlight all of them. If your molecule does not contain any chiral carbons explain why none of the carbons are chiral. One a...
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...
2-methylocta-4,6-dien-1-amineAssignment 1: Draw your molecule from IUPAC
name Using the given IUPAC name, draw your molecule Complete the cover page (p.1) of your portfolio with the
following:o Structural formula of the moleculeo IUPAC name Use a thin, clear binder or report cover to protect the
portfolio Submit the following in the binder:o Cover page as described above (page 1)Assignment 2: Formula, Molar Mass and Functional
Groups On a page titled Expanded Structural Formula draw the expanded
structure of themolecule.o Show...
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