question 8 Analyze the reactant(s) and reaction conditions, then predict the structure of the major organicproduct and indicate the predominant mechanism (SN1, SN2, El, or E2) of cach reaction.CH,CH,CH,CH,Br(CH;),COH, 82°C2 CH;CH;CH;CH;BrNa OCH;CH,OH, 0°C3Na SCH,CH,DMF, 0 CCH3INANO2CH35 CH;-C-OT.CH,H,022° CCH3CH,OHBr22" CCH,(CH:),COH, 82°BrCHạICH3SH43° CCINa OCH,CH,CH;CH,OH, 78° CCH3H,022° CNa OCH,BrCH;OH, 0C

Answered: CHI CH,SH 43° C

Science

Chemistry

CHI CH,SH 43° C

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter21: Benzene And The Concept Of Aromaticity

Section: Chapter Questions

Problem 21.43P: Following is an equation for iodination of toluene. This reaction does not take place. All that...

See similar textbooks

Related questions

Q: CO3(aq) NiCl3(aq) -->

A: Equation

Q: CH2(CO2C2H5)2 NAOC2H5 KOC(CH;)3 B CH3CH2B. CH3I

A: The NaOC2H5 and KOCCH33 will be act as base that will abstract an acidic proton from the given…

Q: केळे वट के वण्य कलनएवन्नজा डि Cटक्d oड कe ककाषु टनप्रट १rज्पि ल कैकट कोनककब Coमालपलव . धोण् औ्रैकट…

A: In this question, we will find out the type of peak splitting pattern for methylene hydrogen. You…

Q: 2. CaCl2 (aq) + K2CO3 (aq) -->

A: The required solution is as follows:

Q: Q:2 Provide a systematic name for each of the following compounds a b d C2CHCHB. Cl,CCH,Br Cl e f…

A: In (E) nomenclature, the higher priority groups are at opposite position.

Q: Solve the attached Problem.

A: organic reaction mechanism is the basic tool to learn the organic reaction

Q: c) .CI NH3

A: Since the N in NH3 has a lone pair electron and the carbon in the reactant which is making bonds…

Q: о + 3 от H CH₂CH₂CH₂ II H 1. POH, H,0, 2. 6 но

A: This Reaction is Aldol Condensation which takes place in presence of Base .

Q: HFag) HSO, (aq) F (aq) 7.

A: This is an example of acid base reaction.

Q: 1. 2. 3. 4. 5. HC1 + CH3I -CH3 + HONO N-H + a N- -H NHCH3 + HONO

A: Here we have to write the major product formed in the following given reactions.

Q: с) S,2- d) NC13 e) C2H4 f) CH3OH

A: THE LEWIS STRUCTURE The Lewis structure depicts a molecule's valence shell electron…

Q: f. g. H3C SH CH3

A: Dear student, As you have asked multiple question and which question has to be answered is not…

Q: Na, NH3 CH3CH3OH

Q: CHEM 111 Nomenclature Lab 2C 2)b. K3ASO4 d. Caз(РОa)2 f. Na2SiO3 h. K2Cr2O7 j. KMNO4 1. L12SO4 n.…

A: 2) b. K3AsO4 - Potassium Arsenate

Q: d) OCH2CH3 CI + CH3CH3OH2 +Cl +2 CH,CH;OH e) + NH, NH2 + 2 NH3

A: Tertiary halides involve in SN1 reaction in which carbocation intermediate is formed by leaving the…

Q: . Fe . ΗΝO3 FeCla + HCI + H2S → • K2C12O7 + KI + H3PO4 H2 + H2O + S NO 12 + CPPO4 K3PO4 + H2O +

Q: 3) OCH3 OCH3 ОН @ H Т. H CH3 -OCH3 (f) Cl Н Н

A: To give the IUPAC names for the following compounds. Few points to keep in mind while naming a…

Q: CH3 CH3 TH 3LOCOCOCCH3 H3NCCOCH2 PH Et, N

A: Protection of amine group:

Q: -CHs HC но CH3 LOCH3 H3C NO2 CH SH

A: IUPAC naming of the given organic compounds. As per our guideline we have to answer first three…

Q: 4. Pb + H3(PO4) → H2 +_ Pb3(PO4)2 -- 5. Li3N + NH4 (NO3) - LINO3 + (NH4)3N - 6. HBr + Al(OH)3 → H20…

Q: f) d) HC HC CH3 CH3 CH HC

A: IUPAC name of given compounds are as follows

Q: NAOCH3 CH;OH `OCH3 a) (88%) OCH3 NaOCH, b) н снон CH;OH `OCH3 ÓH (72%)

A: Nucleophilic Addition Reaction: In this type of reaction, a nucleophile adds to an electrophilic…

Q: What is the identity of FA 3? O A. C18:0 O B. C15:1 O C. C14:2 O D. C20:0

A: Retention time for all five Fatty acids are as below: Fatty acid 1 = 4.176 Fatty acid 2 = 6.004…

Q: 1.) (CH3)2CuLi 2.) CH3B 3.) H3O+

A: step 1 is nucleophilic attack of organometallic reagent (CH3)2CuLi . this attack is at 4th position…

Q: CH12 O2 H2O C,Hs O2 CO H20 C,Hs O2 C H20

A: The reactions given are,

Q: CH3 H. SH NH2 CI NO2 CH3 CI. OCH3 OCH2CH3 O2N NO2

A: We have to Provide a name for the following given molecules below in step 2 as follows :

Q: a) 2 CI 2 Na Br NaOC2H5 / DMF b) (CH3CH2)2CuLi/DMF c) CI CH3OH

A: Organic synthesis is a special branch of chemical processing which concerns the deliberate formation…

Q: CH3 CH;CH,CI AICI3

A: Given

Q: 3) What is the relationship between the compounds shown below? CH3 it: H OH H CH3 H OH H. CH3 OH CH3…

Q: CI CI CH3- CH CH2 CH CH2 - CH2 C2H5

Q: он H2SO4 (cat.) HO Ph

A: See product in red box.

Q: Br, FeBr, SOCII, -OH OH PBr3

A: Since you have posted a question with multiple sub-parts, we will solve the first three subparts for…

Q: (a) C2H2 (b) cis-C2H2Cl2 (c) trans-C2H2C12

A: Since you have posted a question with multiple sub-parts, we will solve first three subparts for…

Q: NECCH,CH3

A: Select principle carbon chain containing functional group Numbering Naming (prefix + word root +…

Q: H. (CH3),CBr AIBT3

Q: В. HI CH2 с. „CH3 Cl2 CH3 1. ВНз D. CH3 2. H2Оz, ОН- CH3

A: B. Alkene reacts with hydrogen halide to form haloalkane. The reaction proceeds in two steps.

Q: COOH OH Mirror image HO CH3 (1) (II) Draw the flying wedge representation of a. its mirror image…

A: Chirality- a compound which have its non-superimposable mirror image to each other called chiral…

Q: CH3C CH2 CH3 + CH3OH 3D OH %3D

A: Aldehyde and ketone reacts with nucleophilic addition reaction with alcohol molecule in the presence…

Q: who ОН cat. Me H;C HO CH3 2 H3C

A: This is a condensation reaction with CO2 production.

Q: H₂ [(COD)(Cy3P)IrPy]PF6 BuOH dax |||

A: The catalyst given in the reaction is called as a crabtree's catalyst. It is a controllable cationic…

Q: Which compound in each pair is the stronger acid?

A: Strong Acids: The acids that dissociate completely into its ionic form will act as strong acid that…

Q: 1. 2. CO2H co,H CH,C= CCH=CHCO2H CH3CHCH2CH2CHCH3 4. CH3 CH3CN 3. CO2H 5. CN NC .CO2H 6.

Q: CH,CH(CH3)2 Cstlu 4 3 2 1 CCH2CH2CH2CH3 14 42CHC=

Q: -CH3 2 CH3NH2 h. H3C-CH,-

Q: CH3 CH3 + OCH3 a. + CI OCH3 OH + I b. OH LOCH2CH3 + OCH,CH3 + CI с. d. Br CN CN + Br +

Q: acid FÓRMULA pKe1 pK.2 pK23 pK«4 Он HO-C-CH2-C–CH2–Ĉ–OH 2.94 4.14 5.82 16.0 0=C-OH

A: HA <===> H+ + A-

Q: COOCH3 OH Br делзеный дух ОН NH CI CH3 CH3

Question

question 8

Analyze the reactant(s) and reaction conditions, then predict the structure of the major organic
product and indicate the predominant mechanism (SN1, SN2, El, or E2) of cach reaction.
CH,CH,CH,CH,Br
(CH;),COH, 82°C
2 CH;CH;CH;CH;Br
Na OCH;
CH,OH, 0°C
3
Na SCH,CH,
DMF, 0 C
CH3I
NANO2
CH3
5 CH;-C-OT.
CH,
H,0
22° C
CH3
CH,OH
Br
22" C
CH,
(CH:),COH, 82°
Br
CHạI
CH3SH
43° C
CI
Na OCH,CH,
CH;CH,OH, 78° C
CH3
H,0
22° C
Na OCH,
Br
CH;OH, 0C

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Step by step

Solved in 2 steps with 2 images

SEE SOLUTION Check out a sample Q&A here

Similar questions

Following is an equation for iodination of toluene. This reaction does not take place. All that happens under experimental conditions for the formation of radicals is initiation to form iodine radicals, I , followed by termination to reform I2. How do you account for these observations?
Trichloroisocyanuric acid, TCICA, also known as “swimming pool chlorine,” is a stable solid that oxidizes alcohols, following a mechanism similar to oxidation by HOCl. No reaction occurs between TCICA and the alcohol (in a solvent such as acetonitrile) until one drop of HCl(aq) is added, whereupon the reaction is over in a few minutes. Write the mechanism for this oxidation that shows the key role of the acid catalyst. Show the oxidation of just one alcohol, not three.
Molecule: 6-chloro-4-ethylhex-2-enoic acid For the mechanism you will focus on the reaction of the portion of the molecule drawn only (not the R part). For any corrections, disregard the parts of your molecule represented by R-groups. Below the incorrect mechanism write a discussion (step-by-step) of the incorrect mechanism identifying all of the mistakes in the mechanism. Keep in mind that there will be more than one mistake in the given mechanism and that the product given is not necessarily the correct product of the reaction of your molecule with the given reagent. For each mistake, give a detailed, scientific explanation of why it is incorrect. Draw your own correct mechanism on a new page
ORGANIC CHEMISTRY - PERICYCLIC REACTIONS Indicate the products, no need to design the mechanisms.
Assign these reactions as SN1, SN2, E1 and E2 on the blank line on the right side of the reactions
Add these 2 equations and obtain an overall reaction (cancel out compounds that appear in the reactants of one equation and the products of the other euaqtion and vice versa producing an overall equation reaction) (CH3)2SiCl2 +2H2O ----> (CH3)2Si(OH)2 +2HCl n(CH3)2Si(OH)2 -------->[(CH3)2SiO]n + nH2O
C3H6 + H2O + H2SO4 --> C3H8O + H2SO4 what is the catalyst in the reaction above?
Predict the products and mechanisms of the following reactions. When more than oneproduct or mechanism is possible, explain which are most likely. 2-chloro-2-methylbutane + NaOCH2CH3 in ethanol
Write the products A, B, C, D, E, F, G, H, I, J and K in the following reactions.
Predict the products and mechanisms of the following reactions. When more than oneproduct or mechanism is possible, explain which are most likely. ) 1@bromo@1@methylcyclopentane + NaOEt in ethanol
Are there any other possible products for the following reaction in catalytic H2SO4 and H2O?
This is the type of organic reaction wherein a single reactant splits into two products and is accompanied by the formation of a small molecule. addition substitution elimination condensation What is the name of the angle that a nucleophile approaches the carbon on the C=O bond? Borge-Dante Bürgi–Dunitz Baran-Daly Bunsen-Debye