dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. Ignore any inorganic byproducts. Br CH₂ONA, CH₂OH heat
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- CH vary анги ans Que soven 3 ΜΟΝ TUE WED FRI THU SAT SUN a 3-methylpentane is for colourless liquid TIME characteristic smell that reacts with a with bromine legried (a diatomic catalyst, a s one molecule) in the presence of 3-methylpentane riquid A bromo 3-m formed through the compound hydrogen with brom: Subsitution of one ->wrike a balance equation for this reaction and explain of it requires gas ga Balancing It drogen bromide gove abon also a product of this rensence of cabayst woke O SEARCH plololololo uld you exp во св th + mars 11 bo your 17 https://learn2.open.ac.uk/mod/ouc ceerrrrrrr romine che13:27 ll 4G O. The following presented reaction scheme lead to the synthesis of which major product from benzene, assuming separation of products is possible? soj 1. NaOH Cl Product - Product H,SO, 2. H,0 FeCl OA Meta-Chlorophenol O B. para-ChloroSulfenic acid OC. Para-Chlorophenol OD. Meta-chloroaniline Add a caption... > Status (Custom)What is the major organic product of the following intramolecular Friedel- Crafts Acylation reaction? - CI AICI వ- డెవదిద్దడ -CI OI 0 1 8 || OIV OV IV
- PLEASE HELP SHOW STEP BY STEP ELECTRON FLOW MECHANISM FOR THE FLOWING REACTION STEREOSELECTIVE ALKENE SYNTHESIS BY THE HORNER-EMMONS REACTION H (EtO), PCH,Ph (EtO),PCH₂Ph cat. BuчN* Br 50% NaOH hexanes ?6. Complete reaction scheme below indicating reagents, catalysts and conditions, and side product trigil bezinslog si6101fon 290b 1l (b Senines levirba 6 gaubong nasamots gniwollot ads to doinW 01 sniowl (6 CH3 40 CH3 Scansgowi (d Ege nodie) ( nsgyxo (b NO₂ 19m02 2i gniwollet sits to mainW II HOpt pt pt 1 pt C|Chec C Chee C I need 8 https://east.cengagenow.com/ilrn/takeAssignment/take CovalentActivity.do?locator-assignment-take b Answe F3 • You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. [References] Draw the structure of the one tertiary (30) alcohol with the molecular formula C5H120. Submit Answer F4 90-85 4+ F5 ¤- CHA 95 IF6 C Draw *+ a O. IF F7 C/C MOTION EYE C Draw F8 SONY Draw F9 C Home WEB k ak DISPLAY F10 F11 C-Draw C One Touch Web Access Withc
- divls depends oin the moisture content of the reaction mixture. Propose a detailed mechanism for ench of the following steps to account for the observed The outeome of oxidation of alkenes with 1odine and silver acetate to afford stereochemistry of the product HO () 2, 2 RCO2Ag (i1) NaOH (aq) HO HO () 2, RCO2Ag, H20 (11) NaOH (aq) HO(a) Provide the missing reagents and line structures of the products (C- E) for the following reactions. Include stereochemistry for products Cand E as indicated. No mechanisms are required. (5) C H,0 Show stereochemistry any one diastereomer OH PCC. CH;Cla D H. Pd/C Show stereochemistry any one enantlomerFor each compound, give the product(s) expected from (1) HgSO4>H2SO4@catalyzedhydration and (2) hydroboration–oxidation.(a) hex-1-yne
- EXPLAIN THE MECHANISM OF EACH REACTION 3. Hydrogen Addition- Selectivity CH₂ H₂C- Catalyst CH₂ HH 4. Mechanism of Catalytic Hydrogenation H H Alkane product ⒸThomson-Brooks Cole -H Pd H H Hydrogen adsorbed on catalyst surface Regenerated catalyst H₂C CH₂ H H C C LIZ Complex of alkene to catalyst Η Η΄ CH₂ H H H Insertion of hydrogen into carbon-carbon double bond(a) For the reaction of 1-methoxy-4-methylbenzene with CH3C(O)CI in the presence of AICI3, describe the bonding and electron distribution in 1-methoxy- 4-methylbenzene, formation and structure of the electrophile in the reaction, and the most stable intermediate responsible for the end product. i H3C1 CI, AICI 3 Me- -OMe 1-methoxy-4-methylbenzene (b) Use phenol as the substrate, propose a synthetic scheme to produce 2-allyl-4-bromophenol (Mechanism not required). Br OH OH phenol 2-allyl-4-bromophenol (c) Propose a synthesis of Compound A starting from benzaldehyde and other necessary reagents of your choice (Mechanism not required). OH CHO CI. Compound A benzaldehyde (d) For the given 13C NMR chemical shifts of the carbonyl carbons in the order of ketones > aldehydes > carboxylic acids, provide an explanation. O CH3 H3C. 13C NMR Chemical Shifts: H₂C1 H₂C H > OH 200 ppm 181 ppm 209 ppmch Complete the following reactions by providing the missing products and reagents A-G. i) ii) iii) OH H₂PO4 heat Attach File O C E 2 0 N m-CPBA 1. LDA 2. HBr Pravics Local Cilac Br A ♫ D F 99+ a 1. Mg 2. O 3. H₂O+ B G N