Determine the reagents required to convert (CH3)2C=CHCOCH3 to each product. [1) [1] 1] Li (1] Br CuLi [2] H20 [2) H20 12] H,0 oH Izl (2) H,0 А. В. OH С. OH
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![Determine the reagents required to convert (CH3),C=CHCOCH3 to each product.
[1]
[1]
[1]
1]
Br
[1]
CULI
[2] H2O
(2] H,O
2) H,0
[2] H,0
2) H,0
В.
OH
С.
OH
A.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F8cdf6e6d-9527-44f6-950f-65997f5f298f%2F8a63a649-cfc7-47ee-a6a6-5218f24c358a%2Fptpxvl_processed.jpeg&w=3840&q=75)
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- Which group in each pair is assigned the higher priority? a. – CH3, – CH2CH3 b. – I, – Br c. – H, – D d. – CH2Br, – CH2CH2Br e. – CH2CH2Cl, – CH2CH(CH3)2 f. – CH2OH, – CHOWhat is the product (A, B, C, or D) of the reaction shown in Image30? a. C b.D c. B d. A1. Which among these would be the most stable carbocation?a. Allylicb. Vinylicc. Primaryd. Secondary2. What is the primary reason for the stability of tertiary carbocations?a. Free rotationb. Resonancec. Hyperconjugation
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- reactions and products for C9H8O4 C9H8O4 + O2 --> C9H8O4 + H2O --> C9H8O4 + HCl --> C9H8O4 + OH- --> C9H8O4 + Na --> C9H8O4 + F -->Draw the products of the following reactions. Use curved arrows to show where the pair of electrons starts and where it ends up. a. ZnCl2 + CH3OH b. FeBr3 + Br c. AlCl3 + Cl−Which reaction corresponds to the Kb for HSO4− ? a. H2SO4 ⇌ H+ + HSO4− b. SO42− + H2O ⇌ OH− + HSO4− c. HSO4− + H2O ⇌ OH− + H2SO4 d. HSO4− ⇌ H+ + SO42− e. HSO4− + OH− ⇌ H2O + SO42−
- A hydrocarbon of unknown structure has the formula C8H10. On catalytichydrogenation over the Lindlar catalyst, 1 equivalent of H2 is absorbed. Onhydrogenation over a palladium catalyst, 3 equivalents of H2 are absorbed.(a) How rnany degrees of unsaturation are present in the unknown?(b) How many triple bonds are present?(c) How many double bonds are present?(d) How many rings ar e present?(e) Draw a structure that fits the data.a. Draw three-dimensional representations for all stereoisomers of 2-chloro-3- methylpentane, and label pairs of enantiomers.b. Considering dehydrohalogenation across C2 and C3 only, draw the E2 product that results from each of these alkyl halides. How many different products have you drawn?c. How are these products related to each other?The Hofmann product is favored by the E2 mechanism when 2-bromo-3-methylbutane is added: A. MeOH B. MeO:- in MeOH C. Nal in acetona D. (CH 3)3 CO:- in (CH 3),COH