Homework Answers
1. In case of alkanes if you replace any one of the H-atom with chlorine atom you will get the same molecule.
2. Here also in case of alkanes like ethane if you replace any H-atom from Carbon 2 you get the same molecule, but in case of alkenes if you already have one chlorine atom in one of the carbon and you replace the H-atom in the 2nd atom, you get isomers on replacing the different H-atom on the Carbon 2
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H-CH Chloroalkane Isomers Molecular Formula Structure Compound Name Hн Hi-C-C-H Ethane CHO HH HCI CH,CI 1-...
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...
question 6b through question 9 please! thank you so much 6. a. Name each of the...
question 6b through question 9 please! thank you so much
6. a. Name each of the structural isomers of CH.. H H H H HHH | | H- C— C C— H H— C— C— C— C— H IH H- C- H H H H H - b. For each structural isomer of CH draw and name the structural formulas for all of its monochloro isomers. Check your answers with models. Does the number of monochloro isomers for each CH,...
stion 2 of 26 Three structural isomers have the formula C, H. Draw and name the...
stion 2 of 26 Three structural isomers have the formula C, H. Draw and name the isomers using IUPAC names. Draw the isomer of CH 2 that has five carbon atoms in the main chain. Select Draw Rings More Erase name of the isomer with 5 C atoms in the main chain: about us | Careers privacy policy terms of use contact us help n2 of 26 > Draw the isomer of C,H,2 that has four carbon atoms in the...
help Part A: Molecular Modeling 1. Models of 1,2-Dibromoethene Br, H Br Br C= C H...
help
Part A: Molecular Modeling 1. Models of 1,2-Dibromoethene Br, H Br Br C= C H Br trans-1, 2-dibromeoethene cis-1, 2-dibromoethene A (trans) B (cis) Figure 7.2. Geometric Isomers. Procedure Part A Construct a model of 1,2-dibromoethene (CHBr=CHBr) so that if viewed from above and in front, see Figure 7.2. Answer all questions on report sheet. 1. Are the models superimposable? 2. Are A and B stereoisomers? Are they enantiomers or diastereomers? 3. Name A, use the E-Z system. 4....
Questions 7-15 The molecule is ethane 71 2 O ACTIVITY 1.2.1 Biological Macromolecules in 3-D 7....
Questions 7-15 The molecule is ethane
71 2 O ACTIVITY 1.2.1 Biological Macromolecules in 3-D 7. Orient the two molecules so that portions of the mo lecules that would normally form intermolecular bonds lie next to each other. In this activity, you will build molecular models of biologically important molecules using ball-and-spring molecular model 1) What intermolecular forces help to hold these mo- building kits and then you will view these and other molecules lecules together! of interest using computer-generated...
____ 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...
Page Chemistry 107 Midterm II Review Problems Draw a Lewis structure for CaHN (think over the...
Page Chemistry 107 Midterm II Review Problems Draw a Lewis structure for CaHN (think over the bonding preferences of each atom when you lay out the skeleton of this molecule!) 1. CC Determine the geometry at each "central atom" (a) Does this molecule have any polar bonds? Is the entire molecule polar? (b) What will be the dominant intermolecular force in a sample of this compound? (c) (c) If you had 100.0 g of this compound, how many moles would...
I have completed some answers! I just really really need help with the rest! I am...
I have completed some answers! I just really really need help
with the rest! I am so lost! please help me, if you can!
What information do you need? Can you see the pictures that I
posted?
#2-6 are using the FIGURE from question #2
#7-8 go together and uses #7 FIGURE
#9-12 uses #9"s FIGURE but #11 and #12 compares the two FIGURES
from #7	
#13 and 14 are together
# 15 and # 16 are their own problems...
My homework is due tomorrow and I have work! Please help me and answer these questions!...
My homework is due tomorrow and I have work! Please help me and
answer these questions! I'll give a thumbs up!
Electronic Structure of Atoms 1.20 Write the ground-state electron configuration for each atom. After each atom is its atomic number in parentheses. (a) Sodium (11) (b) Magnesium (12) (c) Oxygen (8) (d) Nitrogen (7) 1.21 Identify the atom that has each ground-state electron configuration. (a) 1s 2s 2p 3:23p (b) 1:2 2:22 1.23 How many electrons are in the...
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...
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...
question 6b through question 9 please! thank you so much
6. a. Name each of the structural isomers of CH.. H H H H HHH | | H- C— C C— H H— C— C— C— C— H IH H- C- H H H H H - b. For each structural isomer of CH draw and name the structural formulas for all of its monochloro isomers. Check your answers with models. Does the number of monochloro isomers for each CH,...
stion 2 of 26 Three structural isomers have the formula C, H. Draw and name the isomers using IUPAC names. Draw the isomer of CH 2 that has five carbon atoms in the main chain. Select Draw Rings More Erase name of the isomer with 5 C atoms in the main chain: about us | Careers privacy policy terms of use contact us help n2 of 26 > Draw the isomer of C,H,2 that has four carbon atoms in the...
help
Part A: Molecular Modeling 1. Models of 1,2-Dibromoethene Br, H Br Br C= C H Br trans-1, 2-dibromeoethene cis-1, 2-dibromoethene A (trans) B (cis) Figure 7.2. Geometric Isomers. Procedure Part A Construct a model of 1,2-dibromoethene (CHBr=CHBr) so that if viewed from above and in front, see Figure 7.2. Answer all questions on report sheet. 1. Are the models superimposable? 2. Are A and B stereoisomers? Are they enantiomers or diastereomers? 3. Name A, use the E-Z system. 4....
Questions 7-15 The molecule is ethane
71 2 O ACTIVITY 1.2.1 Biological Macromolecules in 3-D 7. Orient the two molecules so that portions of the mo lecules that would normally form intermolecular bonds lie next to each other. In this activity, you will build molecular models of biologically important molecules using ball-and-spring molecular model 1) What intermolecular forces help to hold these mo- building kits and then you will view these and other molecules lecules together! of interest using computer-generated...
____ 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...
Page Chemistry 107 Midterm II Review Problems Draw a Lewis structure for CaHN (think over the bonding preferences of each atom when you lay out the skeleton of this molecule!) 1. CC Determine the geometry at each "central atom" (a) Does this molecule have any polar bonds? Is the entire molecule polar? (b) What will be the dominant intermolecular force in a sample of this compound? (c) (c) If you had 100.0 g of this compound, how many moles would...
I have completed some answers! I just really really need help
with the rest! I am so lost! please help me, if you can!
What information do you need? Can you see the pictures that I
posted?
#2-6 are using the FIGURE from question #2
#7-8 go together and uses #7 FIGURE
#9-12 uses #9"s FIGURE but #11 and #12 compares the two FIGURES
from #7	
#13 and 14 are together
# 15 and # 16 are their own problems...
My homework is due tomorrow and I have work! Please help me and
answer these questions! I'll give a thumbs up!
Electronic Structure of Atoms 1.20 Write the ground-state electron configuration for each atom. After each atom is its atomic number in parentheses. (a) Sodium (11) (b) Magnesium (12) (c) Oxygen (8) (d) Nitrogen (7) 1.21 Identify the atom that has each ground-state electron configuration. (a) 1s 2s 2p 3:23p (b) 1:2 2:22 1.23 How many electrons are in the...
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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