Create a synthesis that starts from acetylene, benzene, coz, Na cN, NaN 3, of four or fewer and products. or simple alcohol carbons. Show all mechanisms О 0 Br
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- please provide product, mechanism and name of reactionPredict the products for the following reactions by showing complete reaction mechanisms. Also, identify the nucleophilic attack, loss of leaving group, proton transfer, rearrangement in the mechanism steps. Show curved arrows in the reaction mechanisms.The following reaction can be carried out in two steps. Choose the correct reagents i) and ii) to perform the following reaction. CN i) 11) or Oi) CN; ii) heat Oi) CN ; ii) H₂O, acid catalyst O i) Br₂; ii) CN- O i) H₂O, acid catalyst; ii) CN O i) HBr; ii) CN
- Consider the following reaction: AIC Toluene MECOCI Me- COME TICI How are these products being formed? Show all appropriate steps (mechanism) in this reaction. Show all appropriate arrows!!!And can u show with the arrow formalism? And can u pls tell me what the role of Hcl and H2O is.? Thank uwhat will be the product formed.explain mechanism
- In each reaction box, place the best reagent and conditions from the list provided. 1) Br 2) 3) 4) DEET (the active ingredient in over the counter insect repellant) 5) Answer Bank Mg, Et,0 HN(CH, CH, ), (1 equiv.) H,O* CH,COOH CH,CH,NH, CH,CH, Br NH(CH,CH,),(2 cquiv.) НСООСH, H,CO НСООН CH, CH, OH NaCN NaNH, Br,, FeBr, SOCI, CO,Organic chemistry qu( do first 3 with mechanism )
- owing reactions proceeds via an SN1 or SN2 of the reaction: (b) S2 pro85 39 Br tort atubong auonsV HMPAnoitutitaduaThe following reaction can be carried out in two steps. Choose the correct reagents i) and ii) to perform the following reaction. CN Oi) H₂O, acid catalyst; ii) CN Oi) HBr; ii) CNT Oi) CN; ii) H₂O, acid catalyst i) CN; ii) heat i) Br₂; ii) CN .A mechanism for the reaction of bromine with 4,4-dimethylcyclopentene in water is shown below. Which of the following statements about this mechanism is correct? Step 1 Br Br Br + Br Br Step 2 Br ;OH OH2 Br Br XX .. Step 3 + Hо HO:) H. O In Step 1, bromine could add to the other face of the alkene, giving a bromonium ion that is the enantiomer of the one shown. O In Step 2, water could attack the other carbon atom of the bromonium ion, leading to the enantiomer of the product shown. O This mechanism is complete and correct. O In Step 2, water could attack the bromonium ion from the other side, leading to the cis product.
