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- The order from most reactive to least reactive with aqueous ammonia is (А) CH--o-č-CH, * CH,--oCH,CH, * CH,--a CH--č-OCH,CH, ° CH,--c³ CH---o-č-CH, > CH3-C-OCH2CH3 | CH3-C-CI | (В) %3D > CH3-C-CI CH3-C-0-C-CH3 (C) > CH3-C-CI CH3-C-OCH2CH3 CH3-C-0-C-CH3 (D) || > CH3-C-CI CH3-C-0-C-CH3 CH3-C-OCH2CH3Cl H H I -H Identify the 'cartoon' drawing of the donor orbital in the nucleophilic substitution reaction of ethanoyl chloride with LiAlH4. Η Al H H CI H III H H IV H H ΑΙ H ہے A B መ II C D || III IVclassify the following reaction C2H6 + O2 -- CO2 + H2O
- Write down the common (not IUPAC) names of the organic molecules that would be released if this molecule were hydrolyzed: CH₂ E CH CH,−O O || 11 O -(CH₂)7-CH=CH-CH₂-CH=CH-CH₂-CH=CH-CH₂-CH3 (CH₂)7 -CH=CH-CH₂-CH=CH-CH₂-CH=CH-CH₂-CH3 -(CH₂)16-CH3 Separate each name with a comma. You will find useful information in the ALEKS Data resource. a × Y Śiii) 5 L. For each of the following El-elimination reactions, draw the step-by-step mechanism (first loss of the leaving group and then proton transfer): H₂O MeOH +=Y OH H.50, HeatНО с оснгенз Cool H+ + H20 он Н20
- H-C- OH Does the equilibrium lie to the left or to the right in the following reaction: Н-С—ОН + CH,-Ö:- ċ-0 + CH,-ö-H ??Mechanism: A reaction mechanism for the following reaction is shown below. H+ CEN CEN: N-H || -C-OH H₂O, H* Step 1 wand woled mot ozsm E Step 3 N-H C-OH C=N-H Step2 C=N-H H-O-H H₂O motno vgiene fesrigid onlt to smotnos -C=N-H a) The overall reaction is an example of b) Step 1 is c) Step 3 is d) Draw in the curved arrows for each step. e) Identify the nucleophiles and electrophiles where appropriate. f) Fill in the reaction energy diagram. H₂O: rate determining step to noipojovo hamwell sit 5(emise erit voittons 10) vanas mi sdgin al rainW di of E^ reaction progress →The cis and trans 2-butene stereoisomers have the following rate constant values associated with the electrophilic addition of water in an acid medium at the same temperature. what is the difference between the two values through the energy profile of each reaction. CH3 H,O productos H+ H3C k = 3.51 x 10- M's1 H3C CH3 H,0 > productos H+ k = 8.32 x 10®M's1
- 31. Which mechanism is correct for the following intramolecular substitution reaction? (a) (b) (c) 4- H-N H H N: H H₂N N: он --مرح CI CI CI H H CI N: NaOH N: CI *H :OH -- NH NH CNH на он NH NHWhat is the classification for this reaction? SO 3 + H 2O → H 2SO 4double replacementdecompositioncombustionreplacementcombination600 500 400 Reactant 300 画 200 E, = 435 10J 2 100 아-- Initial state AE-7X 10 J -30 0° 30 60 90 120 150° 180 210 Reaction progress (angle of twist) Cis-2-butene is one of two forms of butene where the middle two carbon atoms are joined by a double bond. The other form is trans-2-butene. The conversion of the cis form to the trans form is slow at room temperature, and the two forms represent two distinct compounds. Conversion of the cis to the trans form involves rotation about the C-C double bond, which requires a substantial amount of energy on the molecular scale. Move the slider to observe the different conformations and their energies along the pathway of the conversion. Consider the linkage between the two central C atoms in cis-2-butene. How many sigma bonds join these two C atoms? Potential Energy 10 J