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- [nine]1) Find AH for the synthesis of B₂H6, diborane: 2B(s) + 3H2(g) → B₂H6(g) Given: 2 B(s) + 1/2O2(g) → B2O3(s) B₂H6(g) + 3 O2(g) →B2O3(s) + 3 H₂O(g) H2(g) + 1/2O2(g) → H₂O(1) H₂O(1)→ H₂O(g) AH₁ = -1273 kJ/mole AH₂=-2035 kJ/mole AH3= -286 kJ/mole 44 kJ/mole AH4=starting from benzene, how might you synthesize these compound
- Question 8 Identify the type of isomer for (5)-3-methylheptane. O Racemic (*) O Levorotatory isomer (-) O Dextrorotatory isomer (+) O Has to be experimentally determinedCyclopropane decomposes fairly rapidly at moderate temperatures whereas cyclohexane is quite stable. Why is this the case?Question 8 Identify the type of isomer for (R)-3-bromoheptane. O Has to be experimentally determined O Dextrorotatory isomer (+) O Levorotatory isomer (-) Racemic (*)
- Write the structure of the organic product in each of the following reactions. If electrophilic aromatic substitution occurs assume only monosubustitution.Compare and contrast the physical and chemical properties of: • propan-1-ol and propan-2-ol; • (E)-butenedioic acid (fumaric acid) and (Z)-butenedoic acid (maleic acid)In the following structure I have abbreviated the long carbon chain as an R group. Provide the two major products of the following reaction (Hint: Must consider stereochemistry!). HO H R H Br₂ What is the isomeric relationship of the two products?