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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 cheWhat was the starting alkyne and the corresponding reagents for the formation of (this is acetylide formation): CH;CH2CH2C=C-H H-C=C–H and NaNH2, NH3 , CH3CH2Br B H-C=C–H and NaNH2, NH3 , CH;CH2CH2CH2B. H-C=C-H and NaNH2, NH3, CH3CH2CH,Br D Н—СЕС—H and NaNH2, NH3, CH;CH2CH2CH,CH,Br6. 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 HO
- Provide the major organic product of the reaction shown. NV L Draw the molecule on the canyas by choosing buttons from the Tools (for bonds), t [1] A OH 4' 1. NaH эсе 2. CH₂CH₂CH₂CH₂I H: 120 EXP. CONT L Marvin JS ? ** I U ZOS CI BrIdentify the major prouct of the folowing sololvsi reaction of 3bromo-1-methyiycopentene with methanol, Br CH,OH to13:27 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)
- 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) HOfonmetion of 3+ (a) The coX (NH3)5 and SCN differ by NO more than a fuctor rate con5tunt for the 12t from forx-Ge, B2 Ng of two.eehat is the mechanism of Substitution?A Studen t is Purformad the falliwing reaction and atter Com plet ing the work-up Step and isulating be cnde Aridunet iP was detenmined they t The starting matunal Was still Hcsent The student attmped to peaty The Aroduet by columo Chamatagraphy wih Slia gel column and ethyl 94tate as the eluant- The studn't Collected 1o fractiuns and ran g TLC of cnch fraction 4 8 9 10 cunclude about the Separatión ? (whch fractiun s What Can yoy Contained which compund? Are there mixed fract win s?)
- 4:31 PM Mon May 8 ← Problem 22 of 30 1) PhMgCl (C6H5MgCl) 2) HCI/H₂O Draw the products resulting from addition of a Grignard reagent to an aldehyde. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, Ignore any inorganic byproducts. CI @ 90% H SubmitWhat i the MAJOR praduct of the reaction below? Ch H3C- - NHČCH3 FeCl - NHČCH; H3C- H3C- - NHČCH; © H;C- - NHČCH, O H3C- - NHCH;Reactions: Provide the structure(s) of the expected maior oreanic productis. Show stereochemistry where needed and write NR if there is no reaction. H2SO4, 1000C heat a. OH OH 1. TSCI, Pyridine 2. NaCN, DMSO b. HO, PCC, DCM с. (CH3);COK d. t-BUOH Cl 1. CH3MGBT, Et,O 2. H;0* C.