find elimination product When 2-spamo-Icyclopnylethene reacts with hydroxide, A The substiutiam praduct is: and the mechorsie...
(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,...
How would I go about solving question 1 in the image?
How would I draw the major products?
I. (24 pts.) Indicate the type of reaction that will predominate (i.e., S1, SN2, E1, or E2), and when draw the structure of the major product when: 1. isopropyl chloride reacts with hydroxide predominate rxn. structure: 3. 2-iodopentane reacts with ethoxide in DMSO predominate rxn. structure: 2. t-butyl tosylate reacts with CH3OH predominate rxn. structure: 4. ethyl bromide reacts with CH30- predominate...
2. (1.5 pts) Label the following reagents as Good or Poor Nucleophiles AND as Strong or Weak Bases. OK Na SH 3. (1.5 pt) Predict the productts) of the following reactions, if there are multiple products indicate which, if any, is the major product. Be sure to clearly mark the stereochemistry of chiral carbon atoms and draw multiple products if there is more than one stereoisomer that forms. HCI MeOH H2SO H2 Pd/BaSO4 quinoline 4. (3 pt) For the following...
3. Shown below are a series of reactions. Predict the major product for each of them. Remember, you will need to first decide whether the reaction occurs by an SN2, SN1, E2, or E1 before you can determine what the product will be. Label each as SN2, SN1, E2, or E1. Hint: First decide whether S2/E2 or S1/E1 is favored, and then decide whether the reaction pathway goes by a substitution or elimination reaction. SN2 / SN1 E2/E1 Na DMSO,rt...
Circle the mechanism (SN2, SN1, E2, or E1) responsible for the formation of each product in this reaction. If the product cannot be formed in the reaction, circle "not a product". (2 pts) ГОН SN2 SN1 E2 E1 S N2 SN1 E2 E1 SN2 SN1 E2 E1 S2 Sn1 E2 E1 not a product not a product not a product not a product
Draw the major E2 reaction product formed when
trans-1-chloro-2-ethylcyclohexane (shown below) reacts with
hydroxide ion in DMSO.
Draw the major E2 reaction product formed when trans-1-chloro-2-ethylcyclohexane (shown below) reacts with hydroxide ion in DMSO.
Predict the major product for the following reaction. Label whether the reaction will proceed through an SN2, Sn1, E2, or E1 mechanism. SN2 / S1/E2/E1 сн. Br NaCN (1 mol) (1 mol) Predict the major product for the following reaction. Label whether the reaction will proceed through an SN2, SN1, E2, or E1 mechanism. SN27 SN1/E2/E1 NaOCH; Сн,он Draw the line structures of the reactants below and predict the product of their reaction. Label the reaction as SN1, SN2, E1,...
Is it right answer for B?
and D E please..
Substitution/Elimination Practice 1. Please identity the type of reaction (SN1, SN2, E1, or E2) and draw the major product(s): Bryty OH NaH DMF SN2 SNI OH NaOEt HOEt ΕΑ
How would I go about solving parts 2,3, and 4 in this
problem? How would I draw the product?
I. (24 pts.) Indicate the type of reaction that will predominate (i.e., SN1, SN2, El, or E4), draw the structure of the major product when: 1. isopropyl chloride reacts with hydroxide predominate rxn. structure: 3. 2-iodopentane reacts with ethoxide in DMSO predominate rxn. structure: 2. t-butyl tosylate reacts with CH3OH predominate rxn. structure: 4. ethyl bromide reacts with CH30- predominate rxn....
Predict the two most likely mechanisms which occur when 2-iodohexane is heated in ethanol. SN2 and E2 SN2 and SN1 E2 and SN1 E1 and E2 E1 and SN1