Is it a correct way to prepare FENCLORAC? And can someone help me to tell me how to do this experimentally in the lab with giving the quantities till reaching the product (FENCLORAC)?
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- (in Consider the tolluiing reactun hat is the theorechial yıcld Product if -50g of Startiny inaturial and o. grams) KoH arc use1? 0:50g f KOH Mdcular wughts 5611 Chemial fomala;(8 Hyo 4olecalar waghts :20-15 Mukalar cuclght:222.29Phm Phn -ph Provide the reagent necessary to Synthes13e the Compounds in 9 myltistep Synthesi3 - Use Autecting groups when necessary. Provide the reagunt heassary to 5 yn the s13e the Compounts 59 mylti step Synthe sis . Use prstectmy grups when nelessaryWe your anver on paper and submit a picture here gir emaitto me ty the end of pe time for he exam CHOH CH.OH CHOH HA Provide a step-wise mechanism for the following equation, show intermediates and arrows for exchange of electrons.
- A eFundi : Home : Overview E NCHE 121 - Module test - Versio X G Which one of the alkenes can for x b My Questions | bartleby + A https://docs.google.com/forms/d/e/1FAlpQLSeaeyD2qYYYa712LcEehfMLha7DEaTq1KXQ5g7o2byUrT8CnA/formResponse Question 4: The alkene 2-methylbut-2-ene reacts with hydrogen cyanide (HCN) to form the Markovnikov product. Write the preferred IUPAC name of the main product of this reaction. [Use lowercase letters. Do not use spaces if it is not required in the name.] * Your answer Question 5: Which statement about electrophilic addition reactions is not true? * Markovnikov's rule explains why the addition reactions of unsymmetrically substituted alkenes are regiospecific. Markovnikov's rule does not apply to internal alkynes. The larger amount of the nucleophile will bond to the more stable carbocation during an electrophilic addition reaction. None of these statements are correct. O All of these statements are correct. Question 6: The mechanism in Figure 6 produces…PPh3, DIAD CH20H (A) THF mitsunobu H2N sreaction NH2 excess AGOH () (Ci3H20 INS) me I N-me mehow can I sintetize methylcyclohexanone?
- ll mobily ? 4:13 PM O 21% O < Homework - carboxylic a... CH3CHCH2CH2CHCH3 CH3CCO2H CH3 (c) .CO2H (d) CH3 CH3CCN CH3 (g) Br (h) CN BRCH2CHCH2CH2CO2H Q2: Draw structures corresponding to the following IUPAC names: (a) cis-1,2-Cyclohexanedicarboxylic acid (b) Heptanedioic acid (c) 2-Hexen-4-ynoic acid (d) 4-Ethyl-2-propyloctanoic acid (e) 2-Cyclobutenecarbonitrile Q3: How could you convert butanoic acid into the following compounds? Write each step showing the reagents needed. (a) 1-Butanol (b) 1-Bromobutane (c) 1-Butene How could you convert each of the following compounds into butanoic acid? Write each step showing all reagents. (a) 1-Butanol (b) 1-Bromobutane (c) 1-Butene How could you convert butanenitrile into the following compounds? Write each step showing the reagents needed. (a) 1-Butanol (b) Butylamine(Brew the Shuctrie of eadh as -1-ethyl-4- methylaydsherane 5. 2,3-dimethyl-4-propylnomane c4-130proppldecane. of the fallowmg a.Homewock (1) When a sample ol 4-heplanone WAS Iradiiled ili 150 = with 1 radiation wath 4 power outpul of 60 W under condria of t absorplion, il w as lound that 3 8 tinial C;L wir md Whte quantum yield for the formalion of etlhen0
- Draw tructural or or he ajor roduct f he eaction shown. CH3CH=CHCH3 Cl2 • Do not show stereóchemist in other cases. • If the reaction produces a racemic mixture, just draw one stereoisomer. • Show product stereochem IF the reactant alkene has both carbons of the double bond within a ring. C. opy P. C. progress ChemDoodle (Previous Submit Answer Retry Entire Group 9 more group attempts remainingLout line a synthesis tor geherating Compand ma as the excusive using Compounds Fan 6. LDA or as your Selečtish ofbases major priduct You may ust only Number es sential Steps as requiree trans farmation the Componndwnte out seven separate reactions of 2-metheyl propene, includivg reagentis) and product e. Include stereochemistny where reberant. 9 Wnte out Fuve separak reachens of propyne, including reagent e) and product , include stereochemistny where relevant.