What is the effect of structure (1º, 2º, or 3º leaving group) on reaction rate of...
Name 1. Classify the following substrates as 1º, 2º, 3º, aryl, allylie, or benzylie: 8 8 xq 2. Identify the substrate, nucleophile/base, and the leaving group in the following reactions and indicate the type of reaction (ie. SN1, SN2, E1, E2) taking place: 3. Rank the following alcohols in order of increasing reaction rate (1=slowest, 4-fastest) in an SNI reaction:
1. Classify each halogen in every molecule below as: 1º, 2º, 3º, allylic, benzylic, vinyl, or aryl. od five 2. Numerically rank the radical species below in order of increasing stability. ki im. ^. its 3. Draw all relevant resonance structure for each of the radical species shown below. oder 4. Predict the major product for the radical chlorination reactions shown below.
Count the 1º, 2º, 3º, and 4º carbon atoms are present in the hydrocarbon below (Write your answer in the box below) - MacBook Pro WHERRAME
14. Place 1º, 2º, 3º and Methyl carbocations in order from least stable to most stable. What factor(s) account for the stability of the most stable species?
CHEM 104L ALCOHOLS AND PHENOLS Oxidation Classification (1º,2º 3º) Color with Line Line Structure KOVO Compound structure of product, if reaction Ferric occurs Com 1-Butanol dark brown Order 1-Hexan Okid 2 Propanol dark brom dark brown dark brour porida 2-Methy A cyclohexanol Oxidizer 2-Methyl-2-propanol nooyida stays case Phenol ourge ho ondo oxidation dark brom Question Which alcohol cannot be oxidized? Is this alcohol primary, secondary ary, secondary or tertiary?
Classify each alcohol as 1º, 2º, or 3º. a. CH3CH2CH2OH 2° alcohol b. (CH3CH2)3COH ( 3° alcohol OH c. [ ( 1° alcohol A
Classify the carbon atoms in each compound as 1º, 2º, 3º, or 4°. Be sure to answer all parts. a: b: 0 o c: d: O [2] Le 1 < Prev 32 of 42 Next > d: d [2] b a: b: c: d: O h b 8 [3] o a: b: c: d: o f: o o h: 0 a https://newconnect.mheducation.com/flow/connect.html Say g e a: b: c: d: lo h: 1. O Prey 320 to search o i
For the following three structures, (a) identify the leaving group, LG, by circling it, and (b) provide the substitution at the alpha carbon, ac, by designating it as either unsubstituted, 1º, 2º, or 3º. I" O= U OMS нан H₃ C-N CH3
Consider a reaction with a 3° leaving group and a strong nucleophile/bad base. What reaction pathway will prevall (SN1, SN2, E1, or E2)? Explain your reasoning.
(3 pt) For the following reactions:
a) Label the substrate (1°, 2°, 3°), reagent (Good/Poor Nu,
Strong/Weak Base) and solvent (protic, aprotic).
b) Determine what mechanism will predominate (SN1, SN2, E1, or
E2).
c) Draw the product(s) you would expect to form, paying
attention to regioselectivity and stereoselectivity.
4. (3 pt) For the following reactions: a) Label the substrate (1º, 2º, 3º), reagent (Good/Poor Nu, Strong/Weak Base) and solvent (protic, aprotic). b) Determine what mechanism will predominate (SN1, SN2, E1,...