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Q: Name of the following compound H.
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Q: What is the correct name for the following compound: H EC- CH3 Br CI H3C
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Q: CH3 Br. Br HgC 三三 name the compound IUPAC
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- Complete the following reaction equations :(i) C6H5Cl + CH3COCl →(ii) C2H5NH2 + C6H5SO2Cl →(iii) C2H5NH2 + HNO2 →Choose the one has the highest priority, and the one has the lowest. (Please show why) -CHO -COOH -COCH3 -CONH2reactions and products for C9H8O4 C9H8O4 + O2 --> C9H8O4 + H2O --> C9H8O4 + HCl --> C9H8O4 + OH- --> C9H8O4 + Na --> C9H8O4 + F -->
- What is the name of this molecule? (look at the picture to be able to answer) a) (Z) -5-bromopent-2-ene b) E) -5-bromopent-2-ene c) (Z) -5-bromopent-2-ol d) (E) -1-bromopent-3-ene cis-5-bromopent-2-ene e) (E) -1-bromo-4-methyl-but-3-enebest condition for the reaction (1r,2s)-1 bromo-2methylcyclohexane->(s)3-methylcyclohex-1ene-Name the correct mechanism via arrow pushing -name each mechanism -name each minor and major products (1S,2R)-1-iodo-2-methylcyclohexane + sodium cyanide/ DMF-->
- Predict the product of this reaction 1. 7-Bromo-3-octene + Cl2 2. 1-Cyclohexene + H2 3. 1-propene + HBr 4. 3-fluoro-2-methylpentane ---> _____ + HF (For Alkene and Alkyne Naming, follow this format “Branch-Carbon Prefix-Functional Group Suffix”) e.g. 3-methylhex-2-enePlease name the following compounds. Make sure you spell each name correctly, leave no spaces since any variations in spelling will result in the loss of points. Example1: (1Z,3E,6Z)-1,6,8,8-tetramethylcyclonona-1,3,6-triene Example2: (Z)-1,6,8,8-tetramethylcyclonon-1-en-3-yne *I started to guess, but please give the correct name for each of the compounds, regardless of what I have typed into the space.*Please help with the following... Draw the bond line structures for the reactants and the products obtained in the following reactions: 1. m-chlorocumene +NaNiPr2, HNiPr2 2. 4-tertbutyl-3-methyl anisole + HNO3, H2SO4 3. o-isopropyl acetophenone + PhCH2COCl, AlCl3
- What is the rate law implied by the mechanism given below? CH3COCH3(aq) + H+(aq) ←→ CH3C(OH)CH3+(aq) (fast, reversible) CH3C(OH)CH3+(aq) → CH3C(OH)=CH2(aq) + H+(aq) (slow) CH3C(OH)=CH2(aq) + Br2(aq) → CH3C(OH)CH2Br+(aq) + Br-(aq) (fast) CH3C(OH)CH2Br+(aq) → CH3COCH2Br(aq) + H+(aq) (fast) A. Rate = k[CH3COCH3][H+] B. Rate = k[CH3COCH3] C. Rate = k[CH3COCH3][Br2] D. Rate = k[CH3COCH3]2 E. Rate = k[CH3COCH3][Br2]/[H+] (Answer is A, looking for explanation why!).Ochem IUPAC names Can you please see if I have named these correctly (see the attached image for the compound structures) I have them named as follows: 1-iodo-4-methoxy-2-nitrobenzene 3-bromo-5-phenylaniline 4-cyclopentyl-2-hydroxybenzoic acid 3-methyl-1-phenylbutan-1-ol If these are incorrect please correct them!KMnO4, warm, conc'd reacts with hept-1-ene to yield __________. CO2, hex-1-ene CO2, hexanoic acid Formic acid, pentanoic acid Ethanoic acid, pentanal Formic acid, hexanone