a)
Interpretation:
Show the mechanism of the formation of dicyclopentadiene from cyclopentadiene, draw the representative unit of the
Concept introduction:
In this process, the addition
In this process, an initiator is added to the reaction mixture. This initiator gets added to the carbon-carbon double bond and yields a reactive monomer (intermediate). This reactive intermediate reacts with the monomer and this process keeps on repeating to give rise to the final polymeric product.
The formation of PDCPD is taking place by ROMP (ring opening metathesis polymerization), an olefin metathesis reaction can be stated as the reaction between two molecules (
The catalyst used for olefin metathesis polymerization is Grubb’s catalyst (it contain a carbon-metal double bond and have a genral structure as M=CH-R. The function of Grubb’s catalyst is to react reversibly with an alkene to form a four membered cyclic compound knowa as metallacycle. Here, “M” is Ru i.e. ruthenium.
Metallacycle opens up in the next step to give rise to different alkene and a different catalyst.
b)
Interpretation:
Show the mechanism of the formation of dicyclopentadiene from cyclopentadiene, draw the representative unit of the polymer containing three monomer units and draw the structure of PDCPD.
Concept introduction:
In this process, the addition polymerization takes place. Addition polymerization is also known as chain growth polymerization.
In this process, an initiator is added to the reaction mixture. This initiator gets added to the carbon-carbon double bond and yields a reactive monomer (intermediate). This reactive intermediate reacts with the monomer and this process keeps on repeating to give rise to the final polymeric product.
The formation of PDCPD is taking place by ROMP (ring opening metathesis polymerization), an olefin metathesis reaction can be stated as the reaction between two molecules (alkenes) by exchanging their substituents on their double bonds.
The catalyst used for olefin metathesis polymerization is Grubb’s catalyst (it contain a carbon-metal double bond and have a genral structure as M=CH-R. The function of Grubb’s catalyst is to react reversibly with an alkene to form a four membered cyclic compound knowa as metallacycle. Here, “M” is Ru i.e. ruthenium.
Metallacycle opens up in the next step to give rise to different alkene and a different catalyst.
c)
Interpretation:
Show the mechanism of the formation of dicyclopentadiene from cyclopentadiene, draw the representative unit of the polymer containing three monomer units and draw the structure of PDCPD.
Concept introduction:
In this process, the addition polymerization takes place. Addition polymerization is also known as chain growth polymerization.
In this process, an initiator is added to the reaction mixture. This initiator gets added to the carbon-carbon double bond and yields a reactive monomer (intermediate). This reactive intermediate reacts with the monomer and this process keeps on repeating to give rise to the final polymeric product.
The formation of PDCPD is taking place by ROMP (ring opening metathesis polymerization), an olefin metathesis reaction can be stated as the reaction between two molecules (alkenes) by exchanging their substituents on their double bonds.
The catalyst used for olefin metathesis polymerization is Grubb’s catalyst (it contain a carbon-metal double bond and have a genral structure as M=CH-R. The function of Grubb’s catalyst is to react reversibly with an alkene to form a four membered cyclic compound knowa as metallacycle. Here, “M” is Ru i.e. ruthenium.
Metallacycle opens up in the next step to give rise to different alkene and a different catalyst.
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Chapter 31 Solutions
EBK ORGANIC CHEMISTRY
- Transmitance 3. Which one of the following compounds corresponds to this IR spectrum? Point out the absorption band(s) that helped you decide. OH H3C OH H₂C CH3 H3C CH3 H3C INFRARED SPECTRUM 0.8- 0.6 0.4- 0.2 3000 2000 1000 Wavenumber (cm-1) 4. Consider this compound: H3C On the structure above, label the different types of H's as A, B, C, etc. In table form, list the labeled signals, and for each one state the number of hydrogens, their shifts, and the splitting you would observe for these hydrogens in the ¹H NMR spectrum. Label # of hydrogens splitting Shift (2)arrow_forwardNonearrow_forwardDraw the Lewis structure of C2H4Oarrow_forward
- a) 5. Circle all acidic (and anticoplanar to the Leaving group) protons in the following molecules, Solve these elimination reactions, and identify the major and minor products where appropriate: 20 points + NaOCH3 Br (2 productarrow_forwardNonearrow_forwardDr. Mendel asked his BIOL 260 class what their height was and what their parent's heights were. He plotted that data in the graph below to determine if height was a heritable trait. A. Is height a heritable trait? If yes, what is the heritability value? (2 pts) B. If the phenotypic variation is 30, what is the variation due to additive alleles? (2 pts) Offspring Height (Inches) 75 67.5 60 52.5 y = 0.9264x + 4.8519 55 60 65 MidParent Height (Inches) 70 75 12pt v V Paragraph B IUA > AT2 v Varrow_forward
- Experiment: Each team will be provided with 5g of a mixture of acetanilide and salicylic acid. You will divide it into three 1.5 g portions in separate 125 mL Erlenmeyer flasks savıng some for melting point analysis. Dissolve the mixture in each flask in ~60mL of DI water by heating to boiling on a hotplate. Take the flasks off the hotplate once you have a clear solution and let them stand on the bench top for 5 mins and then allow them to cool as described below. Sample A-Let the first sample cool slowly to room temperature by letting it stand on your lab bench, with occasional stirring to promote crystallization. Sample B-Cool the second sample 1n a tap-water bath to 10-15 °C Sample C-Cool the third sample in an ice-bath to 0-2 °C Results: weight after recrystalization and melting point temp. A=0.624g,102-115° B=0.765g, 80-105° C=1.135g, 77-108 What is the percent yield of A,B, and C.arrow_forwardRel. Intensity Q 1. Which one of the following is true of the compound whose mass spectrum is shown here? Explain how you decided. 100 a) It contains chlorine. b) It contains bromine. c) It contains neither chlorine nor bromine. 80- 60- 40- 20- 0.0 0.0 TT 40 80 120 160 m/z 2. Using the Table of IR Absorptions how could you distinguish between these two compounds in the IR? What absorbance would one compound have that the other compound does not? HO CIarrow_forwardIllustrate reaction mechanisms of alkenes with water in the presence of H2SO4, detailing each step of the process. Please show steps of processing. Please do both, I will thumb up for sure #1 #3arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
- Principles of Modern ChemistryChemistryISBN:9781305079113Author:David W. Oxtoby, H. Pat Gillis, Laurie J. ButlerPublisher:Cengage Learning
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