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- 7) Which structure below represents a ketone? A) CH3CH2 0– CH,CH3 B) II C- Он C) CH3CH2C H D) -ċ-CH3 E) -NH2Draw the structure of an alkyl bromide with molecular formula CgH13Br that fits each description: (a) a 1° alkyl bromide with one stereogenic center; (b) a 2° alkyl bromide with two stereogenic centers; (c) an achiral 3° alkyl bromide.Which of the following is an acetal? A b с с D d E e c=0 H3C- C CH2 -C-0CH3 Нзс—О— С — ОН A B H3C-OCH2CH2O-CH3 CH-CH3 E
- Which 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;Q5. What product is formed when cyclohexanone is reacted with each of the following reagents? MgBr KCN H30* H30 NABH4 H;O*Draw the product formed when pentanal (CH3CH2CH2CH2CHO) is treatedwith following reagent. With some reagents, no reaction occurs. [1] HC≡CNa; [2] H2O
- Match each reagent to the product that it forms. Multiple reagents may form the same product. нох Reagent Reagents SOCI2, pyridine: C CISO2CH3, pyridine: E HCI: A PCI 3: A A) B) "It "ft "bl H₂O D) E) F) پہلے علی علیہName the following compounds properly, including stereochemistry. CH3 H3C a) b) он Br e leom d Son lasal Br cle e en S) Draw the structures of the following compounds. a) acetonitrile Jud iyrdem snonet b) benzonitrile c) acetic acid d) formic acid outoge e) propyl propanoate y o trans Draw specific (no R's) examples of: the tet a) a hemiacetal b) a phosphorus ylide. c) an acid chloride d) a hydrate The reaction of acetone with NABH4 is a) a hydration b) a hydrolysis c) an oxidation d) a reduction pts) "Soap" may be defined as: a) a long chain carboxylic acid b) the sodium salt of a long chain acid c) the methyl ester of a long chain acid d) an anhydride of a long chain acid8) OH ел 'H HCI H2O W How many stereoisomers are possible for this cyclic hemiacetal? OH
- The major product of the following reaction has the molecular formula C10H1603. Draw its structure in the most stable tautomeric form. 1. NaOC,H; 2. Н,О" С, Н,ОН15-41 Compound A(C5Hh, is not optically active and cannot be separated into enantiomers. It reacts with bromine in carbon tetrachloride to discharge the purple color of bromine and form Compound B( C.FL Br,). When Compound A is treated with H., in the presence of a transition metal catalyst, it is converted to compound C(C5H10). When treated with HC1, compound A is converted to compound DtC.HyCl). Given this information, propose structural formulas for compounds A B, C, and D. Hint: There are at least three possibilities for Compound A and, in turn, three possibilities for Compounds B. C, and D.What is the major product of the following reaction? ||| ا IV I & III NaOH مداد III IV
