-X-X-X- Linear Homopolymer Branched Homopolymer Cross linked Homopolymer -X-Y-X- Linear Copolymer Branched Copolymer I ---x- Cross linked Copolymer X = CH2-CH₂ y=CH₂= = CH
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- Cp2Fe (ferrocene) + C2F4 (tetra fluoroethylene) ―> P What is the product P? Support your answer with suitable explanation. Draw the structure of the product.rseld=17811238&OpenVellumHMAC=b8bd6f341ba6d101abcde6680011004e#10001 ter 11 Homework lem 11.24 - Enhanced - with Feedback 6354 Part A Identify the following as alkanes, alkenes, cycloalkenes, or alkynes. Identify the compounds by dragging the appropriate labels to their respective targets. alkyne alkane alkene cycloalkene Submit Provide Feedback a C AF Request Answer THIS stane CH3 CH3-C=C-CH3 CH3 BAKERY hp C=CH Copyright © 2023 Pearson Education Inc. All rights reserved. | Terms of Use | Priv 2221 Reset Help ST PALM BO 25 OCT 2022 P Pearson AddressIs the following a primary (1o), secondary (2o) or tertiary (3o) alkyl halide?
- 8. Howare theseplated: (25,3R)2bromD3chloro butene (25) 2bromo z chloro butaneCO DE C6H1206+ + 0 H₂O PER PHOTOSYNTHESIS 1 0 C6H₁2O6 + - O O di O OIdentify the type of Reaction -2-butene + Cl2 —> 2,3-dichloropropane -2-Fluorohexane —> 1-hexene + HF -2-hexanol —> 2-hexene + H2O Choices: -Addition Symmetrical -Addition Unsymmetrical -Elimination
- C=CH H20, H2SO4 H9SO4 CH3 Alkynes do not react directly with aqueous acid as do alkenes, but will do so in the presence of mercury(II) sulfate as a Lewis acid catalyst. The reaction occurs with Markovnikov regiochemistry, so the OH group adds to the more highly substituted carbon and the H adds to the less highly substituted carbon. The initial product of the reaction is a vinyl alcohol, also called an enol. The enol immediately rearranges to a more stable ketone via tautomerization. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions H-OH HO: Hjö: C=CH c=CH Hö Hg HgAn alkene having the molecular formula C5H10 is treated sequentially with ozone (O3) and zinc/acetic acid to give the product/s shown. H3C O CH3CHCH + H. Draw a structural formula for the alkene. You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. In cases where there is more than one answer, just draw one. P opy aste [* Previous Next۱:۳۹ + ۹۰ "ll Asiacell| امتحان الشهر الاول الوقت المتبقي 0:12:10 0 ?nucleophiles اختر واحدة أو أكثر a. CH4 (Ob. Br с. Нао d. NH3 e. H2C=CH2 (-)f. OH (+)g. Br h. BH3 التالي ( السابق II
- Announcements-CHM240-201 x Organic Chemistry ← → C app.101edu.co < CELEBRATING 72"F Cloudy x H R Aktiv Chemistry Which is the stereochemical relationship between this pair of molecules? OH HN OH HN OLD x Mal-Francesca A Tantillo-Out X CHM 240 F22 اك Question 47 of 55 4 TY OL JL 8 - x + A) enantiomers. B) diastereomers C) identical compounds D) constitutional isomers E) Not isomers border P DO * O Submit 9:39 PM 9/11/2022 DDraw all of the stereoisomers of 2-chloro-5-methylheptane. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. CI CI CI Select to Edit an Isomer Drawing ΩΙ· Select to Edit an Isomer Problem 1182 of 18 CI Atoms, Bonds and Rings 1110 CI H Charges || CI CL CI 111. Ō CINa, NH3 H3C-C=C-CH3 CH3 H3C° Alkynes are reduced to trans alkenes by a process called dissolving metal reduction. The reaction uses sodium or lithium metal as the reducing agent and liquid ammonia as the solvent. The method is specific in the formation of trans alkenes from alkynes. The method involves two successive transfers of single electrons from the alkali metal to the triple bond, with abstraction of protons from the ammonia solvent. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions .CH3 H-NH2 CH3 :NH2 H3C H3C