Give the IUPAC name for each metal salt of a carboxylate anion: (a) CgHsCO, Li"; (b) HCO, Na"; (c) (CH)2CHCO, K*; (d) (CH;CH2)2CHCH;CH(Br)CH2CHCO2 Na*.
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- Explain why each of the following carboxylic acids cannot be prepared by a malonic ester synthesis: (a) (CH3CCH;COOH; (b) C,H;CH2COOH; (c) (CHa)CCOOH.Draw the products formed when phenol (C6H5OH) is treated with each set of reagents.a. [1] HNO3, H2SO4; [2] Sn, HCIb. [1] (CH3CH2)2CHCOCI, AlCl3; [2] Zn(Hg), HCIc. [1] CH3CH2CI, AlCl3; [2] Br2, hvd. [1] (CH3)2CHCI, AlCl3; [2] KMnO4Name the following carboxylic acid derivatives, giving both a common name and anIUPAC name where possible. (c) PhCH(CH3)COOCH3
- Which ester can be easily condensed with NaOEt to produce B-keto ester salt? (A) Ph-C–OEt (B) СH, CH, ҫ OEt (C) CH;-CH-Ç-OEt (D) CH, 0 Ҫ Н CH; ÖPQ-17. What is the major product of this reaction? (A) H3CO њсоян (B) OH OH (C) OH O H OH OH 1) CH,MgBr (1 eq.) 2) NHÀ -OH (D) онянGive the IUPAC name for each aldehyde. CH, CH;CHCH-C-H a. CH;CH;CH;-C-CH;CHs сно b. c. (CH):CHCH:CH:CHO d. (CH:).CC(CH):CH:CHO Cire the IUPAC ваше for each ketone/ CH3-C- CHCH2CH3 CH2CH3 ČH3 ČH3
- a) b) c) d) type type OEt type SN ₂ HI ether Br₂, H₂O alkere in a) NaOEt/EtOH b) neutralize type elimination Ixp a) cH₂ B‹ b) NaOH you c) aq. malonic Ester Synthesis aq, HCl OHGive the structure corresponding to each name: (a) sec-butyl ethyl ketone; (b) methyl vinyl ketone; (c) p-ethylacetophenone; (d) 3-benzoyl-2-benzylcyclopentanone; (e) 6,6-dimethylcyclohex-2-enone; (f) 3-ethylhex-5-enal.Which compound shown below Is an Intermedlate In this reaction? Click on a letter A through D to answer. NaOH (aq.) CI OH HO HO,
- Determine the structures of compounds E through I in the following reaction scheme: 1. NaNH2 E H20 F CH;OH G NaOH Br2 NAOH I -> TFOH, CF;CH,OH 2. Br HWhich of the following is an acetal? ОН ОН А) H;С—С—ОН B) H;C-Ċ-0CH; OH OCH3 С) НС—С—ОН D) H;C-c-oCH; ÓCH;Which of the following is an acetal? H3C H;C но CH3 CH3 H3C- H3C H3C H3C OH А C A and C B and D A O A, B, and D D B.