Homework Answers
based on the information write the structures of amines
and then both cis and the trans isomers are geometrical isomers and
they are as follows
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Draw one example each of a primary, a secondary and a tertiary amine as well as an ammonium 1. salt. Draw an alkene...
Draw the structures of the following compounds. Classify each compound as a primary, secondary, or tertiary...
Draw the structures of the following compounds. Classify each compound as a primary, secondary, or tertiary amine, or as a quaternary ammonium salt. 3-ethyl-N- 2-methyl-2-propanamine N-methyl-2-propanamine methylcyclohexanamine 1° amine 2º amine O 3ºamine 4º ammonium salt 1° amine O 2º amine 3º amine O 4º ammonium salt ОООО 1º amine 2º amine 3º amine 4º ammonium salt
Draw the structures of the following compounds. Classify each compound as a primary, secondary, or tertiary...
Draw the structures of the following compounds. Classify each compound as a primary, secondary, or tertiary amine, or as a quaternary ammonium salt. 2-methyl-2-propanamine 1 degree amine 2 degree amine 3 degree amine 4 degree ammonium salt N-methyl-2-propanamine 1 degree amine 2 degree amine 3 degree amine 4 degree ammonium salt N-methylpiperidine 1 degree amine 2 degree amine 3 degree amine 4 degree ammonium salt
Draw the structures of each compound listed in Table 1 using dash-wedge notation. Compound Drawing Internal...
Draw the structures of each
compound listed in Table 1 using dash-wedge notation.
Compound Drawing Internal Mirror Plane? Chiral? (Y/N) ADsolute Configuration (RAS) cis-1,3- dimethylcyclobutane trans-1,3- dimethylcyclobutane cis-1,2- dimethylcyclobutane trans-1,2- dimethylcyclobutane 2-butanol Meso-2,3 butanediol Glycine (aminoacetic acid) Proline (model both enantiomers) Isoleucine (choose TWO stereoisomers) 1,3 dichloro-allene (CHCI)
1. Draw structures of one primary alcohol, one secondary alcohol and one tertiary alcohol and give...
1. Draw structures of one primary alcohol, one secondary alcohol and one tertiary alcohol and give the correct name for each structure you have drawn. 2. Describe the difference between alcohols and phenols. 3. Describe the difference between an aldehyde and a ketone, and indicate how each differs from an alcohol Describe what is meant by oxidation and reduction in relation to organic compounds, giving one example of oxidation of an organic compound and one example of reduetion of an...
7. Draw and label both cis and trans isomers of 1-ethyl-4-methylcyclohexane. (10 pt) a. For each...
7. Draw and label both cis and trans isomers of 1-ethyl-4-methylcyclohexane. (10 pt) a. For each isomer, draw the two possible chairs and indicate which of the two will be preferred and by how much (a lot or little). (5 pt) b. Which of the four is considered the most stable (label as "best") and which is least stable ("worst")? (3 pt) c. Clearly label 1,3-diaxial interactions, if present, in any of the conformations? (2 pt) Cis Trans
INSTRUCTIONS: For each of the following organic molecules, you will do the following. A. Draw the expanded form o...
INSTRUCTIONS: For each of the following organic molecules, you will do the following. A. Draw the expanded form of the organic compound. B. Name your organic compound. For organic compounds, #3-7 in addition to instructions 1 and 2, you need to also do the following. D. Label each carbon as primary, secondary, tertiary or quaternary E. Draw the skeletal form of the organic molecule. 1. Organic Compound: CH Structure: name: 2. Organic Derivative: CH,CI Structure: name: 3. Organic Compound CaH...
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)...
____ 1. The diagram below represents serine, a polar, uncharged amino acid. Which functional group gives...
____ 1. The diagram below represents serine, a polar, uncharged
amino acid. Which functional group gives serine its
distinct property?
a. H3
b. CH2OH
c. –H
d. COO–
____ 2. The monomers shown below are monomers for which of the
following natural polymers?
a. polysaccharides
b. plastics
c. DNA
d. proteins
____ 3. Which of the following processes illustrates the production
of a protein?
a. specific code for amino acids --> amino acid chain -->
gene --> DNA --> specific...
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...
Draw the structures of the following compounds. Classify each compound as a primary, secondary, or tertiary amine, or as a quaternary ammonium salt. 3-ethyl-N- 2-methyl-2-propanamine N-methyl-2-propanamine methylcyclohexanamine 1° amine 2º amine O 3ºamine 4º ammonium salt 1° amine O 2º amine 3º amine O 4º ammonium salt ОООО 1º amine 2º amine 3º amine 4º ammonium salt
Draw the structures of the following compounds. Classify each compound as a primary, secondary, or tertiary amine, or as a quaternary ammonium salt. 2-methyl-2-propanamine 1 degree amine 2 degree amine 3 degree amine 4 degree ammonium salt N-methyl-2-propanamine 1 degree amine 2 degree amine 3 degree amine 4 degree ammonium salt N-methylpiperidine 1 degree amine 2 degree amine 3 degree amine 4 degree ammonium salt
Draw the structures of each
compound listed in Table 1 using dash-wedge notation.
Compound Drawing Internal Mirror Plane? Chiral? (Y/N) ADsolute Configuration (RAS) cis-1,3- dimethylcyclobutane trans-1,3- dimethylcyclobutane cis-1,2- dimethylcyclobutane trans-1,2- dimethylcyclobutane 2-butanol Meso-2,3 butanediol Glycine (aminoacetic acid) Proline (model both enantiomers) Isoleucine (choose TWO stereoisomers) 1,3 dichloro-allene (CHCI)
1. Draw structures of one primary alcohol, one secondary alcohol and one tertiary alcohol and give the correct name for each structure you have drawn. 2. Describe the difference between alcohols and phenols. 3. Describe the difference between an aldehyde and a ketone, and indicate how each differs from an alcohol Describe what is meant by oxidation and reduction in relation to organic compounds, giving one example of oxidation of an organic compound and one example of reduetion of an...
7. Draw and label both cis and trans isomers of 1-ethyl-4-methylcyclohexane. (10 pt) a. For each isomer, draw the two possible chairs and indicate which of the two will be preferred and by how much (a lot or little). (5 pt) b. Which of the four is considered the most stable (label as "best") and which is least stable ("worst")? (3 pt) c. Clearly label 1,3-diaxial interactions, if present, in any of the conformations? (2 pt) Cis Trans
INSTRUCTIONS: For each of the following organic molecules, you will do the following. A. Draw the expanded form of the organic compound. B. Name your organic compound. For organic compounds, #3-7 in addition to instructions 1 and 2, you need to also do the following. D. Label each carbon as primary, secondary, tertiary or quaternary E. Draw the skeletal form of the organic molecule. 1. Organic Compound: CH Structure: name: 2. Organic Derivative: CH,CI Structure: name: 3. Organic Compound CaH...
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)...
____ 1. The diagram below represents serine, a polar, uncharged
amino acid. Which functional group gives serine its
distinct property?
a. H3
b. CH2OH
c. –H
d. COO–
____ 2. The monomers shown below are monomers for which of the
following natural polymers?
a. polysaccharides
b. plastics
c. DNA
d. proteins
____ 3. Which of the following processes illustrates the production
of a protein?
a. specific code for amino acids --> amino acid chain -->
gene --> DNA --> specific...
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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