Fill in the expected organic products: Part: 0/2 isobutyric acid OH HC-CH-CH-Br a H Part 1 of 2 Draw the structure of a. Skip Part Check Click and drag to start drawing a structure. b G Save For Later Submit Assignme 00 E 000 Ar
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- A ALEKS - Alec Nema - Learn G Arrange the compounds below ir x A www-awu.aleks.com/alekscgi/x/Isl.exe/1o_u-lgNslkr7j8P3jH-IvUrTNdLZh5A8CnG03PBGuXr8iCPa7ZMmym9pTWPGPMQBZuhqGO-ia6eFgZ0OQdKyhK7Uw7cw-OpH... ☆ : Apps Sprouts Academy. 9 Online Tutoring C 400 Request Heade... Q Weather & Soil CH.. O CHEMICAL BONDING Predicting the relative ionic character of chemical bonds Alec V Arrange the compounds below in decreasing order of the jonic character of the bonds in them. That is, pick 1 for the compound with the most ionic bonds, pick 2 for the compound with the next most ionic bonds, and so on. jonic character compound of bonds dla CaCl, (Choose one) ▼ Cl, (Choose one) ▼ SiCl, (Choose one) AICI, (Choose one) ▼ Explanation Check O 2020 McGraw-Hill Education. All Rights Reserved. Terms of Use | Privacy I Accessibi 3:5 12/ P Type here to search (15 IIPlease don't provide handwritten solution .....OBr a) Heptanamide 1) (Ме)CuLi b) Mel IC CHCOMe 2) Н.О -OH (aq) c) 2 Acetaldehyde Benzene d) Valeramide SOCI Heat c) 2-Octanone + (Ph):P-CH2
- 1:39 17. Provide the major organic product of the reaction shown. Ph O 1. Et-MgBr (xs) 2. H₂O+ Actual S Sen celAcid-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.Draw the products
- URGENT!!I will rate, pls need this. no need of long explanation.10:58 9 Aa 10:58 AM, Apr 24 Save Share II Using hüterials show & as Staring hukerials show e syvethesis that gets this produet surethusis benzene NO2ll 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
- Which of the following provides a synthetic route to convert 3-iodo-2-methyl-1- butene into 2-methyl-2-butene? 1. NaOH; 2. H₂, Pt 1. H₂, Pt; 2. Br2 1. H₂, Pt; 2. NaOEt 1. H₂, Ni₂B; 2. KOtBu 1. H₂, Pt; 2. KOtBuOAc AcO. OAc Pb N: OAc AcO. COAC N: OAc Pb AcO LOAC ÓAc NH -HOAC Pb H. N: OAc LOAC Pb -HOAC Organic and I norganic Products b.) Pb(OAc)2 + N2 (2 equiv) + Pb(OAc)2 + N2 (2 equiv)+ d.) c.) N: Pb(OAc)2 + Nz (2 equiv) + Pb(OAc)2 NH2Give clear detailed Solution with explanation needed..give answer all sub parts if you not then don't give answer