10- For the following scheme, if the center compound alkene as shown, Give one actual example for the conversion of this alkene to these shown compounds: Alcohol, alkane, diol, dihalides, etc. Show the condition, of temperature, pressure, and the catalysts needed (if any) for each reaction. OH Halohydrin ** 1,2-Dihalide Halide H OH Alcohol Alkene Alkane Epoxide HO он 1,2-Diol C=O Carbonyl compound Cyclopropane
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- An alkene having the molecular formula C11H20 is treated sequentially with ozone (O3) and zinc/acetic acid to give the product/s shown. CH;CH2ČCH,CH3 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. C opy aste ChemDoodleces to access important values if needed for this question. Complete the equation for the following reaction by drawing a structural formula for the missing organic product. CH3CH2NH2 H20 CH,CH,C-OH • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Draw cations and anions in separate sketchers. P. opy aste C. [F Visited CH4 M) M) M) ChemDoodle Submit Answer Retry Entire Group 5 more group attempts remaining17) Which of the following reaction(s) is(are) incorrect? а. Ortho Para Meta CH, CH3 NO, CH3 CH3 HNO, H,SO, `NO, NO, p-Nitrotoluene (37%) o-Nitrotoluene m-Nitrotoluene (59%) (4%)
- n of Halogens to Alkenes 1 pts 2req Draw a structural formula for the product formed upon hydroboration/oxidation of the alkene below. 1 pts (M) CH3 enation of Alkenes CH;CH c=CH2 on of Hypohalous Acids to Alk..1 pts (M) esis of Halohydrins from Alke... 1 pts CH3CH ercuration of Alkenes 1 pts 2req ČH3 vnikov Hydration of Alkenes 1 pts M • Use wedge and hash bonds ONLY for rings. • Do not show stereochemistry in other cases. • If the reaction produces a racemic mixture, just draw one stereoisomer. poration of Alkenes 1 pts 2req n on n C P opy aste larkovnikov Hydration of Al. 1 pts 2reg .. ion of Alkenes: Oxymercur. 1 pts 2req e Reactions: Hydrogenati. 1 pts 2req ide Formation Reaction 1 pts 2req oxylation of Alkenes: Epoxi.. 1 pts 2reg olysis of Alkenes 1 pts 2req ture Determination: Identifi. 1 pts 2req e Nomenclature 1 pts 2req ChemDoodle rophilic Addition to Alkynes 1 pts 2reqC=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 HgA docs.google.com Aug TIle * السؤال الخامس Question - 5 Write the main products for the following reactions: 1- 3-methyl-1-butene + hydrogen bromide - COOH 2- + N2OH 3- 4 - CH;CH2CH2CHOHCH; + Pl3 COOH 5- + 2[H] 6- Methanioc acid reacts with methanol 7- CH3CH,CH,CHOHCH, + O, 8- CH;CH;CH;CHOHCH3 + (0] 9- CH3CH;CH;COCH3 + 2[H] (H+] 10- CH3CH2COOCH3 + H20 1 Add file Вack Next Clea * submit passwords through Google Forms. This form was created inside of Al-Farabi University Col Report Abuse Geogle Ferms
- (a) 2-methyl-2-pentanol Draw the structure of the alkene that was used to prepare the alcohol in highest yield. ? ChemDoodle Which process does this employ? 1. Hg(OAc)2, H₂O; 2. NaBH4 1. BH3; 2. H₂O2, NaOH OsO4, H₂O2 √ [FAn alkene having the molecular formula C,H12 is treated sequentially with ozone (O3) and zinc/acetic acid to give the product/s shown. CH3CH2CH,CH½CH2CH 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 NextWhen the alkene A was treated first with Hg(OAc)2 in MeOH and second with NaBH4 the product was the ether B. Using curved arrows please give the mechanism for the first step of (Hg(OAc)2 in MeOH) this reaction, including any regioselectivity or stereoselectivity. H3C 1. Hg(OAc)2, MeOH H3C O-CH3 =CH2 ✓ -CH3 H3C 2. NaBH H3C A B
- Give the condensed structure and the IUPAC name of the product/s for each of the following reactions and indicate for each the mechanism involved in the formation of such produc/s as SN1, SN2, E1, E2 a. CH;CH;CH;Br + LIAIH, b. (CH3),CBr + CH; CH;OH, heat at 60 C c. BrCH;CH2CH,Br + Mg(ether)IV. Complete the equations for the following reactions. Show all organic alkene products form, mechanism, indicate the major product and the rule Ş(CH3)2 NaSH HEAT OH™ HEAT34. Which molecule is the most reactive in an Ssz reaction? (A) CH,CH;CH:CI (B) CH3CH;CH;0H (C) CH,CH;CH,OTs (D) CH3CH;CH,CN