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- In the light-catalyzed alkane chlorination mechanism, the first stage (first step) consists of the cleavage t DY -C-H »r ܘܘ: ܘܘ: ܀ X- + :Q -:+ *@ ܘ: ܘ: :ܘ: ܘ:a) Complete the following reactions: (i) H3C-C-Ci + H2O A + B (ii) HO H;C. CH3 SOCI, с + D + so, (iii) H;O* HCN E F CH;CH, `CH;3 (iv) CH;CH,CH,CH,CH,Br + NH3 G + H excessWhich of the following methods can be used to synthesize 2-methyl-1-hexene, shown below, with no formation of isomeric by-products? ОН H2SO4 A) heat H2SO4 OH B) heat Ci (CH3);CO Na* + D) H2C=P(C,H5);
- 5. Consider the synthesis of 2-butanone from butyne: Hg2+ || CH3CH,-C=C–H CH;CH,-Ĉ-CH3 H3o* (iv) Name the class of compound D belongs to. (v) Comment on the stability of compound D compared to 3-butanone.4 C following Friedel-Crafts reaction? ( B OMe A What is the product of the H AICI, OMe OMe OMeIt's ET2CuLi sorry haha!! I just would like to know what the major product would be! Thanks sm!
- 5. which of the following compaunds wendd be more sin th. eguilibrium (*aplain tha rentu e) HC f) 3) "C R 14 R= CH3 CH2 CH2Which of the following represents a step in the mechanism for the alkoxymercuration of 1-methylcyclopentene in methanol? с O View Available Hint(s) O O A B C Hg" (OAc) D Hg" (OAc) B D Ho(OAc) Hg (OAc) CHR R 200 R H H [1] Nu: [2] H₂O R 'R' st ↓ X H₂SO4 CH3CH2OH NaNH, NaNH, (2 equiv.) NaNH, (2 equiw 1. NaCN 2. H₂O
- 5-52 The following syntheses have flaws in them. What is wrong with each? (a) .CH3 .CO2H 1. Cl2, FeCl3 2. KMNO4 CI (b) CІ CI. 1. (CH3)3CCI, AICI3 2. KMNO4, H2O CO2H4. Draw structures for products of the following reactions. PaCl, (Bu water tBu PdCI, methanol OH CHCI, NaOH, water Me,N LDA, THE, 0°C BulI (2 moles) Bri THF, -78°C Buli THE, °C Br Pd(OAch THE, 0C MeOPlease help with 4c, 4d, and 4e. We havent learned kaw of equivalents so please do 4c a different way. thank you