Curved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the intermediate and product in this reaction sequence. Include all lone pairs and charges as appropriate. Ignore any inorganic byproducts. H-Br: Select to HBr $ Select to Draw Br: Br
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- Please help with 4c, 4d, and 4e. We havent learned kaw of equivalents so please do 4c a different way. thank youA compound X is bitter in taste. It is a component of washing powder& reacts withdil. HCI to produce brisk effervescence dur to colourless, odourless gas Y wich turns lime water milky due to formation of Z. When excs of CO2is passed, ilkinessdisappears due to formation of P. Identify X, Y, And Z & P.3) wite down the open structures of A, B, C and D wfth the reactions the Tyn thes is D, scheme showing given in synthesis the of trust. of pheromone H-CミC- H 1) NANH2 l18quid NHg -78°C. 2) 1- bromo-5-methyl hexone 3(Cg Hgb) 1) NANH2//iquid NHs/-78 °C A (CaHi6) 2) 1-bromodecane P-2 (Nez B)/He . cicuHu) CiHg Cog H D(Cig H3pO) 19 19 CS CamScanner ile tarandı
- what is an is... [Review Topics] Draw the structure of 3,4-diethyl-5-methylheptane in the window below. • You do not have to explicitly draw H atoms. орy aste ChemDoodle Submit Answer Retry Entire Group 9 more group attempts remaining A -1) 1544565- NH₂ 2) CI of & 7) 8) reagents used: FeCl3/Cl₂ HNO3/H₂SO4 MeCI/AICI3 ACCI/Et₂N SO3/H₂SO4 Pd/C, H₂ NaOH H₂SO4/heat ACCI= CI [Choose ]All attempts to isolate primary and secondary nitroso compounds result solely in the formation of oximes. Tertiary nitroso compounds, however, are stable. Explain.
- Acid-catalyzed hydrolysis of a nitrile to give a carboxylic acid occurs by initial protonation of the nitrogen atom, followed by nucleophilic addition of water. Review the mechanism of base-catalyzed nitrile hydrolysis in Section 20-7 and then predict the products for each reaction below and write all of the steps involved in the acid-catalyzed reaction, using curved arrows to represent electron flow in each step.GINE REASONABLE SYNTJE SËS OF THE INDICATED PeoDuCTS FROM THE GIVEN STARTING MATERIALS, Snow STERE OCHE M - ISTRY WHERE IT IS RELEVANT (*), AND SHOW ANY INTER - MEDIATES THAT COULD BE O THER REAGENTS You DEE M FIT, AS LONG A5 THHE-i MAKE CHEMICAL SENSE ARE STABLE ENOUGH TO EXIST, ISOLATED. You MAY usE ANí PhGive answe of both question just with small explanation Asaap Thanks
- cmplete the reacting by adding necessrt reagents. write in thapce provided. make sure to write regents in chemical formula . n separate regents with comma & space (ex. h2so6, h202)What is the name of the following compound +1 Br Brill.. |||| OH₂ OH₂ Co Br H₂O OH₂ trans-teraaquadibromocobalt(1) bromide trans-teraaquadibromocobaltate(1) bromide Ocis-teraaquadibromocobalt(1) bromide cis-teraaquadibromocobaltate(1) bromideGive the major organic product(s) of the following. Include stereochemistry when applicable. 1) Nal Br a) 2) NaCN, acetone 1) NaOC(CH3)3, heat d Br 2) BH₂ THF; 3) H,O,, NaOH(aq) b) c) d) c) 2) KOC(CH3)3, heat Copyright University of California Merced 2022 Br 1) NaOH, heat 2) MCPBA 1) KOC(CH3)3, heat 2) H3O+