CH3 Br2 CH2Cl₂ CH2CH3 Draw the molecules on the canvas by choosing buttons from the Tools (for bonds), Atoms, a appropriate stereochemistry by choosing the dashed or wedged buttons and then clicking a 05 H± 12D EXP. CONT . 134 H с N ° S CH3 Cl Br I P CH3 न क H₂C Br Br H₂Cu Br ΔΟ Од F
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- chem 534 cha Hư OAC H please show stereochemistry H₂ COCH ? H CO₂CH3 O Ac 2. + ? hv 9 40°C 3. H₂ C 4. 0°C Catq Q-0 + [6+4] NGC ?. لك 5. [ V-CO₂CH3 + II NCCN [4+2] C6H5 6. 2 C6H58A eFundi : Home : Overview E NCHE 121 - Module test - Versio X G Which one of the alkenes can for x b My Questions | bartleby + A https://docs.google.com/forms/d/e/1FAlpQLSeaeyD2qYYYa712LcEehfMLha7DEaTq1KXQ5g7o2byUrT8CnA/formResponse Question 4: The alkene 2-methylbut-2-ene reacts with hydrogen cyanide (HCN) to form the Markovnikov product. Write the preferred IUPAC name of the main product of this reaction. [Use lowercase letters. Do not use spaces if it is not required in the name.] * Your answer Question 5: Which statement about electrophilic addition reactions is not true? * Markovnikov's rule explains why the addition reactions of unsymmetrically substituted alkenes are regiospecific. Markovnikov's rule does not apply to internal alkynes. The larger amount of the nucleophile will bond to the more stable carbocation during an electrophilic addition reaction. None of these statements are correct. O All of these statements are correct. Question 6: The mechanism in Figure 6 produces…
- " ΟΝ Ο CON|OU|G fic | G b C COU app.101edu.co Tube Maps > > 2 W X |2|GD|QC| GA W |G1|CS|UO N Question 15 of 31 Provide the correct IUPAC name for the skeletal (line-bond) structure shown here. Stereochemistry is ignored. 4- 5,5- 3- 3,3- 2- 5- di sec- ISO tri cyclo tert- oct meth hex 99 MacBook Air F6 F2 3 E 80 F3 > $ 4 R Aav D₂ % 5 0 모 F5 T 6 Y & v lo 7 F7 U 00 * 8 DII F8 - 9 F9 0 EE 0 G B F10 ☆ Done G PThe AH° values of each compound is given below as kJ/mol. Calculate the entaphy change (AH) value of the following reacti on? 2CaOg) + 2SO2 (g + Ozg) →2 CasO41) -635.5 -296.9 0.0 -1432.7 (kJ/mol) A) 500.3 kJ B) -500.3 kJ С) -1000.6 kJ D) 2365.1 kJ E) -1094.1 kJGive detailed Solution with explanation needed
- please do 5-10C П W Co X А) I В || I Ш E D) IV. "ОН none of these ОН 11 ОН "О H3O* OH OH + enantiomer ||| IV H 7 OF5. Consider the synthesis of 2-butanone from butyne: Hg2+ || CH3CH,-C=C–H CH;CH,-Ĉ-CH3 H3o* (iv) Name the class of compound D belongs to. (v) Comment on the stability of compound D compared to 3-butanone.