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1. Describe properties about alkenes and alkynes. 2. The two stereoisomers of l-bromo-1,2-dichloroethene cannot be designated...
these are the phrase options Part Build models for the two isomers of 1-iodo-1-propene, then complete...
these are the phrase options
Part Build models for the two isomers of 1-iodo-1-propene, then complete the sentences that describe these models. CH I CHE cis-1-iodo-1-propene trans-1-iodo-1-propene Match the phrases in the left column to the appropriate blanks in the sentences on the right. Make certain each sentence is complete before submitting your answer. View Available Hint(s) Reset chiral with superimposable mirror images 1. Try to manipulate the cis and trans isomers of 1-iodo-1-propene rotating bonds, but without breaking bonds....
PROBLEM 7-24 1. Predict the elimination products of the following reactions. When two alkenes are possible,...
PROBLEM 7-24 1. Predict the elimination products of the following reactions. When two alkenes are possible, predict which one will be the major product. Explain your answers, showing the degree of substitution of each double bond in the products. 2. Which of these reactions are likely to produce both elimination and substitution products? (a) 2-bromopentane + NaOCHz (b) 3-bromo-3-methylpentane + NaOMe (Me = methyl, CH3) (C) 2-bromo-3-ethylpentane + NaOH
PROBLEM 7-24 1. Predict the elimination products of the following reactions. When two alkenes are possible,...
PROBLEM 7-24 1. Predict the elimination products of the following reactions. When two alkenes are possible, predict which one will be the major product. Explain your answers showing the degree of substitution of each double bond in the products. 2. Which of these reactions are likely to produce both elimination and substitution products? (a) 2-bromopentane + NaOCH3 (b) 3-bromo-3-methylpentane NaO (c) 2-bromo-3-ethylpentane NaOH Me (Me= methyl, CH3)
Chapter 11: 1. What is a prime rule in naming alkenes? a. Find the longest carbon...
Chapter 11: 1. What is a prime rule in naming alkenes? a. Find the longest carbon chain. b.Find the longest carbon chain containing the alkene. c. Find whether the alkene has a cis- or trans- configuration. d.Find how far the alkene functionality is from either end. 2. What is the IUPAC name of the following alkene? a. cis-5-methyl-2-heptene b. trans-2-ethyl-4-hexene c. trans-5-methyl-2-heptene d. trans-3-methyl-5-heptene 3. What is the hybridization, geometry, and bond angle of the carbon marked by an asterisk?...
Procedure B. 1. Build two models of 1, 2-dimethyleyclopentane. The two methy can be on the...
Procedure B. 1. Build two models of 1, 2-dimethyleyclopentane. The two methy can be on the same face or opposite faces of the ring. No matter how t molecule is twisted, they cannot be superimposed on each other. These compounds are stereoisomers of each other. 2. When two groups are present, the prefix cis (same face) or trans (opposite face) can be used in IUPAC nomenclature to specify which stereoisomer is being considered. For drawings, a solid wedged line in...
please solve them clear & be sure thank you . 1. (21 points) Is the following...
please solve them clear & be sure thank you .
1. (21 points) Is the following compound a meso-compound? If yes, show it in 3D in the box below using wedged and dashed bonds to indicate the substituent bond direction and draw the internal mirror plane of symmetry (if any). (3 points) HOOC-CHOH-CHOH-COOH Draw the 3D structures of the stereoisomers of the compound above. Use wedged and dashed bonds to indicate the substituent bond direction in each stereoisomer. [Hint: if...
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...
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)...
Please Hurry up ?? CHOOSE THE CORRECT ANSWER Q1] Organic chemistry study (a) Properties of organic...
Please Hurry up ??
CHOOSE THE CORRECT ANSWER Q1] Organic chemistry study (a) Properties of organic compounds (b) Reactions of organic compounds (c) syntheses of organic compounds (d) all above Q2] Tertiary Carbon is (a) carbon atom contact with four carbon atoms (b) carbon atom contact with two carbon atoms (c) carbon atom contact with three carbon atoms (d) carbon atom contact with one carbon atom Q3] One of these compounds contain quaternary carbon atom (a) 2,3-dimethylpentane (b) 3-methylhexane (c)...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23,...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...
these are the phrase options
Part Build models for the two isomers of 1-iodo-1-propene, then complete the sentences that describe these models. CH I CHE cis-1-iodo-1-propene trans-1-iodo-1-propene Match the phrases in the left column to the appropriate blanks in the sentences on the right. Make certain each sentence is complete before submitting your answer. View Available Hint(s) Reset chiral with superimposable mirror images 1. Try to manipulate the cis and trans isomers of 1-iodo-1-propene rotating bonds, but without breaking bonds....
PROBLEM 7-24 1. Predict the elimination products of the following reactions. When two alkenes are possible, predict which one will be the major product. Explain your answers, showing the degree of substitution of each double bond in the products. 2. Which of these reactions are likely to produce both elimination and substitution products? (a) 2-bromopentane + NaOCHz (b) 3-bromo-3-methylpentane + NaOMe (Me = methyl, CH3) (C) 2-bromo-3-ethylpentane + NaOH
PROBLEM 7-24 1. Predict the elimination products of the following reactions. When two alkenes are possible, predict which one will be the major product. Explain your answers showing the degree of substitution of each double bond in the products. 2. Which of these reactions are likely to produce both elimination and substitution products? (a) 2-bromopentane + NaOCH3 (b) 3-bromo-3-methylpentane NaO (c) 2-bromo-3-ethylpentane NaOH Me (Me= methyl, CH3)
Procedure B. 1. Build two models of 1, 2-dimethyleyclopentane. The two methy can be on the same face or opposite faces of the ring. No matter how t molecule is twisted, they cannot be superimposed on each other. These compounds are stereoisomers of each other. 2. When two groups are present, the prefix cis (same face) or trans (opposite face) can be used in IUPAC nomenclature to specify which stereoisomer is being considered. For drawings, a solid wedged line in...
please solve them clear & be sure thank you .
1. (21 points) Is the following compound a meso-compound? If yes, show it in 3D in the box below using wedged and dashed bonds to indicate the substituent bond direction and draw the internal mirror plane of symmetry (if any). (3 points) HOOC-CHOH-CHOH-COOH Draw the 3D structures of the stereoisomers of the compound above. Use wedged and dashed bonds to indicate the substituent bond direction in each stereoisomer. [Hint: if...
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...
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)...
Please Hurry up ??
CHOOSE THE CORRECT ANSWER Q1] Organic chemistry study (a) Properties of organic compounds (b) Reactions of organic compounds (c) syntheses of organic compounds (d) all above Q2] Tertiary Carbon is (a) carbon atom contact with four carbon atoms (b) carbon atom contact with two carbon atoms (c) carbon atom contact with three carbon atoms (d) carbon atom contact with one carbon atom Q3] One of these compounds contain quaternary carbon atom (a) 2,3-dimethylpentane (b) 3-methylhexane (c)...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...
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