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3. Draw the structure of the copolymer produced from vinyl d e copolymer is employed in...
1. Draw the structure of the copolymer produced from vinyl acetate and vinyl chloride. This copolymer...
1. Draw the structure of the copolymer produced from vinyl acetate and vinyl chloride. This copolymer is employed in some paints, adhesives, and paper coatings. 2. Isobutylene, CH25C(CH3)2, is used to prepare cold-flow rubber. Draw a structure for the addition polymer formed from this alkene. 3. Kel-F is an addition polymer with the following partial structure. What is the monomer used to prepare it? - i am not able to post partial structure but I tried to write it out...
Ethylene dichloride (CICH_2 CH_2 CI) and sodium polysulfide (Na_2 S_4) react to form a chemically resistant...
Ethylene dichloride (CICH_2 CH_2 CI) and sodium polysulfide (Na_2 S_4) react to form a chemically resistant rubber, Thiokol A. Draw the structure of the rubber. Draw the structure for the polymer produced from the monomer vinylidene chloride (CH_2 = CCI_2). Draw the structure of the copolymer produced from vinyl acetate and vinyl chloride. This copolymer is employed in some paints, adhesives, and paper coatings.
Questions for Experiment 8: Preparation and Properties of Polymers - Polyester and Nylon 1. Which polyester...
Questions for Experiment 8: Preparation and Properties of Polymers - Polyester and Nylon 1. Which polyester should be theoretically more rigid, the one obtained from ethylene glycol or the one from glycerol? Why? Explain with structural arguments. 2. Draw the structure for the polymer produced from the monomer vinylidene chloride CH-00) 3. Draw the structure of the copolymer produced from vinyl acetate and vinyl chloride. This copolymer is employed in some paints, adhesives, and paper coatings 00CH, CI coc Vinyl...
4. Isobutylene, CH-C(CH), is used to prepare cold-flow rubber. Draw a structure for the ad- dition...
4. Isobutylene, CH-C(CH), is used to prepare cold-flow rubber. Draw a structure for the ad- dition polymer fomed from this alkene.
5-80 4.4 7) What is the product of the following reaction? CHy-C-aa,CH-N 8) Draw the structure of a 4 carbon contai...
5-80 4.4 7) What is the product of the following reaction? CHy-C-aa,CH-N 8) Draw the structure of a 4 carbon containing lactone. CH-CH CH-CH-C-OH 9) Provide the major organic product of the reaction below. CECO Soto o louboin d CH-CH-оH CCFCOH CPCHCOH H (cat.) 0) Which of the following can produce Benzoic acid from benzene? 1) HNO3, H,SO 2) CH,CL. AICI 3) NaNO2, HCl, cold 4) CUCN 1) HNO3, H,SO H 2) Fe, HCI 3) NANO,, HCI, cold 4) CUCN...
11.a) Draw the open chain (Fischer) structure of D-altrose. (1pt) (b) How many chiral centers are...
11.a) Draw the open chain (Fischer) structure of D-altrose.
(1pt)
(b) How many chiral centers are in D-altrose? ______ (1pt)
(c) What is the maximum number of possible stereoisomers whch
can exist for D-altrose? _____ (1pt)
(d) Draw L-altrose in open chain form (use Fischer projection) –
you may use the space above. (1pt)
(e) Use the information above to draw a Haworth projection for
alpha-D-altropyranose. (2pt)
Ruff degradation on a monosaccharide causes C1 to be lost as
carbon dioxide,...
Draw Newman Projections for 360 rotation around C3-C4 bond of 3-isopropylhexane. Label each structure as totally...
Draw Newman Projections for 360 rotation around C3-C4 bond of 3-isopropylhexane. Label each structure as totally eclipsed eclipsed, gauche or anti. Estimate the relative energy of each structure and draw the potential energy diagram | QUESTION 6 Complete the following acid-base reaction and estimate the equilibrium constant: 2 он H2C H2 H2 QUESTION 7 If a solution of a pair of enantiomers has a measured rotation of +15°, and the pure S enantiomer has a specific rotation of +25°, what...
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...
____ 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...
Pre-Laboratory Exercise: Plastics Identification I. List four properties that you will use in lab...
can
someone help me find this information?
Pre-Laboratory Exercise: Plastics Identification I. List four properties that you will use in lab to determine the identity of the polymer samples 2. Describe the density test. What observation will help you determine the density of each polymer? What precautions should be taken in placing the sample in the solutions? 3. Write the name and abbreviation for the six recyclable polymers 2 huetn deisity polyetayene.HDpz poulene: PP 4. Given the list of wavenumber...
Ethylene dichloride (CICH_2 CH_2 CI) and sodium polysulfide (Na_2 S_4) react to form a chemically resistant rubber, Thiokol A. Draw the structure of the rubber. Draw the structure for the polymer produced from the monomer vinylidene chloride (CH_2 = CCI_2). Draw the structure of the copolymer produced from vinyl acetate and vinyl chloride. This copolymer is employed in some paints, adhesives, and paper coatings.
Questions for Experiment 8: Preparation and Properties of Polymers - Polyester and Nylon 1. Which polyester should be theoretically more rigid, the one obtained from ethylene glycol or the one from glycerol? Why? Explain with structural arguments. 2. Draw the structure for the polymer produced from the monomer vinylidene chloride CH-00) 3. Draw the structure of the copolymer produced from vinyl acetate and vinyl chloride. This copolymer is employed in some paints, adhesives, and paper coatings 00CH, CI coc Vinyl...
4. Isobutylene, CH-C(CH), is used to prepare cold-flow rubber. Draw a structure for the ad- dition polymer fomed from this alkene.
5-80 4.4 7) What is the product of the following reaction? CHy-C-aa,CH-N 8) Draw the structure of a 4 carbon containing lactone. CH-CH CH-CH-C-OH 9) Provide the major organic product of the reaction below. CECO Soto o louboin d CH-CH-оH CCFCOH CPCHCOH H (cat.) 0) Which of the following can produce Benzoic acid from benzene? 1) HNO3, H,SO 2) CH,CL. AICI 3) NaNO2, HCl, cold 4) CUCN 1) HNO3, H,SO H 2) Fe, HCI 3) NANO,, HCI, cold 4) CUCN...
11.a) Draw the open chain (Fischer) structure of D-altrose.
(1pt)
(b) How many chiral centers are in D-altrose? ______ (1pt)
(c) What is the maximum number of possible stereoisomers whch
can exist for D-altrose? _____ (1pt)
(d) Draw L-altrose in open chain form (use Fischer projection) –
you may use the space above. (1pt)
(e) Use the information above to draw a Haworth projection for
alpha-D-altropyranose. (2pt)
Ruff degradation on a monosaccharide causes C1 to be lost as
carbon dioxide,...
Draw Newman Projections for 360 rotation around C3-C4 bond of 3-isopropylhexane. Label each structure as totally eclipsed eclipsed, gauche or anti. Estimate the relative energy of each structure and draw the potential energy diagram | QUESTION 6 Complete the following acid-base reaction and estimate the equilibrium constant: 2 он H2C H2 H2 QUESTION 7 If a solution of a pair of enantiomers has a measured rotation of +15°, and the pure S enantiomer has a specific rotation of +25°, what...
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...
____ 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...
can
someone help me find this information?
Pre-Laboratory Exercise: Plastics Identification I. List four properties that you will use in lab to determine the identity of the polymer samples 2. Describe the density test. What observation will help you determine the density of each polymer? What precautions should be taken in placing the sample in the solutions? 3. Write the name and abbreviation for the six recyclable polymers 2 huetn deisity polyetayene.HDpz poulene: PP 4. Given the list of wavenumber...
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