Concept explainers
Interpretation:
It should be explained that why two different products are formed from disrotatory ring closure of (2E, 4Z, 6Z)-octatriene, but only one product is formed from disrotatory ring closure of (2E, 4Z, 6E)-octatriene.
Concept introduction:
Pericyclic reactions are “ any concerted reaction in which bonds are formed or brocken in a cyclic transition state”. There is a single transition state from start to finish, in contrast to a stepwise reaction.
There are mainly three types of pericyclic reactions,
- 1) Electrocyclic reactions
- 2) Cycloaddition reactions
- 3) Sigmatropic reactions
In an electrocyclic reaction “one new sigma- bond is formed or brocken.”
Woodward –Hoffmann rules are the set of rules used to vindicate or predict certain aspects of the stereo chemical outcome and activation energy of pericyclic reactions.
Woodward – Hoffmann rules for Electrocyclic reactions are listed below
Woodward – Hoffmann rules for the configuration of electrocyclic reactions are,
Enantiomers are a type of stereoisomers that have the same molecular formula and constitutions around the atom but differ in their spatial arrangement of groups around the atom.
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Chapter 28 Solutions
Organic Chemistry, Books a la Carte Edition (8th Edition)
- Substance X is known to exist at 1 atm in the solid, liquid, or vapor phase, depending on the temperature. Additionally, the values of these other properties of X have been determined: melting point enthalpy of fusion 90. °C 8.00 kJ/mol boiling point 130. °C enthalpy of vaporization 44.00 kJ/mol density 2.80 g/cm³ (solid) 36. J.K mol (solid) 2.50 g/mL (liquid) heat capacity 32. J.Kmol (liquid) 48. J.Kmol (vapor) You may also assume X behaves as an ideal gas in the vapor phase. Ex Suppose a small sample of X at 50 °C is put into an evacuated flask and heated at a constant rate until 15.0 kJ/mol of heat has been added to the sample. Graph the temperature of the sample that would be observed during this experiment. o0o 150- 140 130- 120- 110- 100- G Ar ?arrow_forwardMechanism. Provide the mechanism for the reaction below. You must include all arrows, intermediates, and formal charges. If drawing a Sigma complex, draw all major resonance forms. The ChemDraw template of this document is available on Carmen. Br FeBr3 Brarrow_forwardCheck the box under each compound that exists as a pair of mirror-image twins. If none of them do, check the none of the above box under the table. CH3 OH CH3 CH2 -CH-CH3 CH3 OH OH CH-CH2-CH- -CH3 CH3 CH3 OH OH CH3 C -CH2- C. -CH3 CH3- -CH2- -CH-CH2-OH OH CH3 none of the above كarrow_forward
- Write the systematic name of each organic molecule: structure Η OH OH OH OH H namearrow_forwardDraw the skeletal ("line") structure of a secondary alcohol with 5 carbon atoms, 1 oxygen atom, at least one ring, and no double or triple bonds. Click and drag to start drawing a structure. : ☐ ☑ ⑤arrow_forwardName these organic compounds: structure name CH₁₂ CH3 - C CH - CH2 || CH3- - CH₂ CH₂ | - - CH3 CH3 2-methyl-2-butene ☐ 3-methyl-1-butyne - CH3 CH. - C=CHarrow_forward
- How many different molecules are drawn below?arrow_forwardWith the reference to a anion A, Label compounds B-F as an isomer or resonance strcuture of A. FOr each isomer indicate what bonds differs from A. Provide steps and undertanding on how you come up with work.arrow_forwardProvide steps and also tips to undertand how to do on my own. Add the correct number of hydrogen atoms for each carbon atom and lone pairs to each oxygen atom.arrow_forward
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