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- Draw a structural formula for 2-methylbutan-2-ol. • You do not have to consider stereochemistry. **** Sn [F ? ChemDoodleⓇCH3 CH₂CH₂C CHCH3 *%8 [.. You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • If there is more than one major product possible, draw all of them. • Separate multiple products using the + sign from the drop-down menu. H₂O ·OO ? Ⓡ ChemDoodle H₂SO4 ? [F <Draw the structure of (Z)-1-bromo-1-chloro-1-butene. • Consider E/Z stereochemistry of alkenes. • You do not have to explicitly draw H atoms. AAVII ? ChemDoodle [F Ⓡ
- ed Draw the product(s) of the following reactions. CH₂CH₂CH₂-CEC-CH₂CH3 -85 • Consider E/Z stereochemistry of alkenes. Separate multiple products using the + sign from the drop-down menu. • If no reaction occurs, draw the organic starting material. II.. - 0 ChemDoodle Na/NH3(1) [ ] کر > 87.Howware these pelatad: (25,3R)2bruma3chloro butane (2R,35) 2bromo 3 choro butane1) 1544565- NH₂ 2) CI of & 7) 8) reagents used: FeCl3/Cl₂ HNO3/H₂SO4 MeCI/AICI3 ACCI/Et₂N SO3/H₂SO4 Pd/C, H₂ NaOH H₂SO4/heat ACCI= CI [Choose ]
- 8. Howare theseplated: (25,3R)2bromD3chloro butene (25) 2bromo z chloro butaneWrite the structure(s) for the organic product(s) of the carbohydrate reaction below. ball & stick v|- + labels HOCH2 CH3 0-Ć-CN dilute aq. HCI HO. ČH3 OH Linamarin • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If two diastereomers are formed, draw both. • If no reaction occurs, draw the organic starting material. • Draw carboxylic acids in neutral (unionized) form. • Use “flat" representations of rings, not chairs, in your drawing. Do not draw your answer as a Haworth projection.Draw the structure of (Z)-4-methyl-2-pentene. • Consider E/Z stereochemistry of alkenes. You do not have to explicitly draw H atoms. opy aste ChemDoodle
- Question 5 (12] 5.1 Provide the line structures of the products K to P in the reactions below. Stereochemistry is required for product L. (7) OH H,SO, Pd/C K 7. Major product only Only one stereoisomer Stereochemstry required NABH, MEOH HCI ZnCl, M NH O.2. Complete the following: Stereochemistry and regiochemistry may be important. type a) NaOH (aq) b) neutralize ➤ OMe a) LiAlH4, ether NMe2 f) b) H3O+ type b) a) HS SH ZnCl2, H+ b) Raney Ni g) type formation of thioacetal/desulfurization HO type Hell-Volhard-Zelinsky Reaction h) CO₂Et type Wittig Reaction H H₂N OEt OH DCC, CH2Cl2 Ph type a) NaH, THF CO₂Et d) b) BnBr, THE CO₂Et c) NaOH(aq); HCl(aq); heat type type HO type (COCI)2, cat DMF CH2Cl2 j) CI type a) NHEN b) LiAlH, THE c) H3O+ CO₂Me CO₂MeName the alkene. Be sure to indicate stereochemistry and use hyphens (-) not endashes (-). H3C-CH2 CH3 H. H. The alkene is named: