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using the bottom reaction, compare with the top reaction and determine what the interemediate and starting material is for the top reaction
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- 0 The target diol is synthesized in one step from 1-methylcyclopentene, but your lab partner exhausted the supply of that alkene. Fortunately, you have plenty of isomers (CH₁) on hand from which to synthesize 1-methylcyclopentene and, ultimately, the diol. Provide the missing reagents and organic structures needed to most efficiently produce the target product. reagent 1 Compound A Draw compound A. Select Draw Rings More с H Compound B Erase reagent 2 Identify reagent 1. reagent 3 H3C.. HO ....|H OHThe following three derivatives of succinimide are anticonvulsants and have found use in the treatment of epilepsy, particularly petit mal seizures. Ph Ph `N' `N' ČH3 ČH3 Methsuximide Ethosuximide Phensuximide Following is a synthesis of phensuximide. CN Ph CN Ph CN 1. NaOH, H2O 2. HC, Н20 NaOEt KCN Ph-CHO cOOEt H cOOEt NC COOEt 3. Нeat Ethyl cyanoacetate (A) (B) Benzaldehyde Ph Ph Ph CH;NH2 НООС СООН Et0oC COOEt `N' (C) (D) ČH3 Phensuximide Methsuximide is formed by a similar pathway to that shown for phensuximide. Draw the structure of the compound that reacts with ethyl cyanoacetate in the synthesis of methsuximide.A is no included
- What are the reactions between propanamide and NaOH, H2O; then H3O+?Draw the following a) N-methylpropanamideb) cis-2-heptenec) 2-hexanone d) butylbutanoatee) 3-chloropentanoic acid f) 2,2-dibromo-butanalg) 2-octanolh) 1-propynei) butylethylmethylamine j) butylpropyletherThe following three derivatives of succinimide are anticonvulsants and have found use in the treatment of epilepsy, particularly petit mal seizures. Ph. Ph `N' ČH3 ČH3 Methsuximide Ethosuximide Phensuximide Following is a synthesis of phensuximide. CN Ph CN Ph CN NaOEt KCN 1. NaOH, H2O Ph-CHO 2. HС, Н20 COOET H cOOEt NC COOEt 3. Нeat Ethyl cyanoacetate (A) (B) Benzaldehyde Ph. Ph Ph CH3NH2 НООС СООН EtOOC COOET `N' (C) (D) ČH3 Phensuximide In the conversion of (B) to (C), draw the structure of the product of step 1.
- 1 2 3 4 5 6 Cr₂03 Base RX 1 20 KNO3 H₂SO4 4 5- Isatoic Nitroisatin anhydride carbonyl O N- Alkyl isatin compound HCI/Zn 2 3 quinoline 4- carboxyl acidOPh OPh D CI Br N E N Но o-SiMeg OH OPh OPh F NH2 Но N Но OH OH A V ( Choose ] Bu4N+ F- МСРВА (Ваyer villager) Mg, then CO2 (Kobe!!!!) NH3 (SNAR) H2S04, Heat (Fisher esterification) 03, DMS (ozonalysis) Choose (Choose ) E [ Choose ) F [ Choose ) B.Arrange the following compounds in decreasing order of acidity * |- CICH2CH2CH2COOH Il - CH3CH2CHCICOOH III – CH3CHCICH2COOH III > I> || O I > II > || O I > I| > II III > || >|
- What type of phosphocompound is this? phosphoenol mixed anhydride phosphoguanidine phosphoanhydride phosphoester ° II II он E- H OH ང ОН H ОНa) b) C) HBr CH3CH₂OOCH₂CH3 1. Hg(OAc)2, H₂O 2. NaBH4 1) BH₂ / THF 2) H₂O2 NaOH (aq) coldWhich of the following compounds is an anhydride? I. II. III. II CH3CO CH3C- CH3COH III IV V 2=01 IV. V. || CH3COOH 0 0 CH3COCCH3