Draw the reactants and products of the following reaction: 3-ethyl-2-heptene + HOH → 3-ethyl-3-heptanol + 3-ethyl-2-heptanol...
Draw the reactants and products of the following
reaction:
3-ethyl-2-heptene + HOH → 3-ethyl-3-heptanol + 3-ethyl-2-heptanol
- Consider how it is possible for two products to form in this reaction, and identify the major product, giving your reasons for both.
- What type of reaction is this classified as?
Homework Answers
ab) Hydration reaction on
alkenes type reaction.
In hydration reaction addition of water on alkenes take place.
OH- of water attached on that carbon which has less hydrogen.and H+ attached that C which has more hydrogen.this called markovnikav rule
Add Answer to:
Draw the reactants and products of the following
reaction:
3-ethyl-2-heptene + HOH → 3-ethyl-3-heptanol +
3-ethyl-2-heptanol...
Alder Re? 9. Draw the two major products for the following reaction. a. Identify each as...
Alder Re? 9. Draw the two major products for the following reaction. a. Identify each as either a 1,2 or 1,4 addition product. b. Write either "thermodynamic" or "kinetic" underneath each one. c. Draw the two resonance structures for the intermediate from which both form H-Br ton nroducts for the following reaction. Draw the the major product or products for the following reaction. Drow the resonance structures for the intermediate from which both form Bra/ hv NBS/ peroxides 11. Give...
Give an IUPAC name for the following compound: (E)-4-ethyl-3-methyl-2-hexene (E)-3-ethyl-4-methyl-2-heptene (Z)-3-ethyl-5-methyl-2-heptene (Z)-3-ethyl-4-methyl-2-heptene (E)-3-ethyl-4-methyl-2-hexene (E)-3-ethyl-5-methyl-2-heptene (2)-4-ethyl-3-methyl-2-h
Give an IUPAC name for the following compound: (E)-4-ethyl-3-methyl-2-hexene (E)-3-ethyl-4-methyl-2-heptene (Z)-3-ethyl-5-methyl-2-heptene (Z)-3-ethyl-4-methyl-2-heptene (E)-3-ethyl-4-methyl-2-hexene (E)-3-ethyl-5-methyl-2-heptene (2)-4-ethyl-3-methyl-2-hexene (2)-3-ethyl-4-methyl-2-hexene (Z)-3-ethyl-5-methyl-3-heptene (E)-3-ethyl-5-methyl-3-heptene
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The term "side reactions" refers to any chemical reaction that can occur that form products other than the desired product. Side reactions can consume the reactants of your intended reaction, and can affect the percent yield of your target product. One possible side reaction produces butyl ethyl ether. Draw the complete reaction mechanism for the formation of butyl ethyl ether as a side product 2 Marks]
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fragment as well as m/z values.
1. Give the synthetic route to form the following product as the major product in an aldol reaction using butanal as a starting substrate. он о 2. Discriminate between the reactants and products by using FTIR 3. Discriminate between the reactants and products by using H-NMR 4. Discriminate between the reactants and products by using C-NMR...
Alder Re? 9. Draw the two major products for the following reaction. a. Identify each as either a 1,2 or 1,4 addition product. b. Write either "thermodynamic" or "kinetic" underneath each one. c. Draw the two resonance structures for the intermediate from which both form H-Br ton nroducts for the following reaction. Draw the the major product or products for the following reaction. Drow the resonance structures for the intermediate from which both form Bra/ hv NBS/ peroxides 11. Give...
Give an IUPAC name for the following compound: (E)-4-ethyl-3-methyl-2-hexene (E)-3-ethyl-4-methyl-2-heptene (Z)-3-ethyl-5-methyl-2-heptene (Z)-3-ethyl-4-methyl-2-heptene (E)-3-ethyl-4-methyl-2-hexene (E)-3-ethyl-5-methyl-2-heptene (2)-4-ethyl-3-methyl-2-hexene (2)-3-ethyl-4-methyl-2-hexene (Z)-3-ethyl-5-methyl-3-heptene (E)-3-ethyl-5-methyl-3-heptene
How to draw products of reaction (Skill builder) Type 1 Type 2 Type 3 1) Using the scheme, determine what is your intermediate. It depends on reactants 2) Type 1: Markovnikoy, no preference for sin and anti- draw two products with wedges and dashes; check rearrangement BH TO Type 2- anti addition only, no need in HOR Markovnikov rule, no rearrangement Type 3-sin addition only, anti-Markovnikow no rearrangement CC formation-Zaltsev rule 3) After you draw products: check if product can...
CHM 2430, s18, HW 4 Due: 11 am, Friday, March 23 Name 1. Can 1-iodo-3-methylbutane be made the reaction of 3-methybutan-1-ol with sodium lodide? Explain (Hint: Start by drawing the structures of the reactant and product then ask and answer the folilowing what type of reaction is this? Are the reactants good choices for this type of reaction?) 2. Two possible synthetic routes to cyclopropyl ethyl ether are shown below Which route, A, B, or both A and B, would...
Predict the elimination products for the following reaction. Identify the major and minor stereoisomers and draw them in the indicated box. This is a possible product, but the two phenyl rings repulse sterically, making this unstable. Consider the other more stable stereoisomer.
2. Draw two possible products for the reaction shown below. Are your products formed as a racemic mixture? Which of your two products do you expect to be the major one? Why? 1 equiv. Br2 THF possible product 1 possible product 2 Possible product 1 a racemic mixture? Yes No Possible product 2 a racemic mixture? Yes No Which would be major? Why?
2. Draw two possible products for the reaction shown below. Are your products formed as a racemic mixture? Which of your two products do you expect to be the major one? Why? 1 equiv. VON Br2 THE possible product 1 possible product 2 Possible product la racemic mixture? Yes No Possible product 2 a racemic mixture? Yes No Which would be major? Why?
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Please identify ALL fragments that would appear in Mass
Spectrometry for both reactants and products and detail each
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