Answer Nos. 7-12 Only.Write only the product and the type of reaction it undergone.Thank you! A t and write the UPAC name of the Major Organic Produa fomedALCOHOLS & ETHERSby e foowng reactions1 entene• H0 H50.CH2 CHICHCH,MgCI + CH,CHCHO –M,01 schioropropane + Sodium hydroxide. CH,CH;CH,CH,COOH • LIAIH, ether5. CH,CH,MGCI + HCHO0CH6 CH,CH;CCH, + CH;C-M9CIH07. Chioroethane + CH;ONa8. Ethane + water _H,50.mondon2 CH,CH;CCH,10. 2moles of 1-propanol 140°CLIAIH, ether11. CH.CHCH;CHOCH,+ LIAIH._ether12 CH,CH,C-OCH;CH,CH, + LiAIHe_ether

Acc. To bartleby policy we can only answer 4 questions

Answered: 7. Chioroethane + CH;ONa a. Ethane •…

Science

Chemistry

7. Chioroethane + CH;ONa a. Ethane • water H,50. . CH,CH;CCH, • LIAIH, 140°C ether 1n 2moles of 1-propanol

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter30: Orbitals And Organic Chemistry: Pericyclic Reactions

Section30.SE: Something Extra

Problem 36AP

See similar textbooks

Related questions

Q: LOGEN COMPOUNDS The chlorination of methane to give CCI, in 5. an example of A) an addition reaction…

A: When chlorine reacts with methane one of the hydrogen is replace by one chlorine atom. Like this all…

Q: How do you know what (chemicals, molecules, substances) to place over the arrow?

A: The reaction is:

Q: (a) (b) (c) ОН -OH OH ? -CH₂OH ? (d) О CHOH CH₂OH ? ? moilosot not in ее 2010 о о (e) H (f) -CH₂CI ?…

Q: 9. Identify all functiona l groups (excluding alkanes) for the given molecule (S) b.count all…

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

Q: Indicate wether the following pairs of compounds are constitutional isomers, diastereomers,…

A: The given pair of compounds is represented as follows:

Q: Although alcohol V gives a single alkene W when treated with POCI, and pyridine, three isomeric…

Q: In what conditions alkene I could be converted to alcohol II: 03, Zn H20 O 1-BH3, 2-H202, NaOH…

A: Hydroboration–oxidation reaction: Alkene gives an electrophilic addition reaction with borane.…

Q: 2 eq CH3CH20H H3O* KMNO4, cold -CH2-CH2-C -H dilute

A: When carbonyl group react with alcohol in acidic medium produces acetals and ketols When aldehyde…

Q: Match each alkene to its heat of hydrogenation.Alkenes: 3-methylbut-1-ene, 2-methylbut-1-ene,…

A: The structures of given compound are shown below:

Q: Q1. Give the structure(s) of the major organic produc(s) of A-H , Show stereochemistry if…

Q: (f) Benzene + 3-phenyl-1-propene, H2SO4, heat -------> ? (g) Toluene +…

Q: H Br H- Br Type of reaction? Isit stereospecific? #of streoisomeric products? Relationshie between…

Q: CH-CH, -ÇH- 24 H3C-CH-CH2 `CH3l 25 CHs -C,H5 26

A: The name for the given structures has to be given.

Q: Can you help me to solve these questions ?

A: Since we only answer one question at a time, we'll answer the first one (Question No. 5). Please…

Q: ठीकरखे +he fनाकायांण खपवमोनक := मo3 Ca9) +[a[जিoम), S) >Vi(No3), ৭৭)+\2-H20 S] aeoptete the icomic…

A: Write the balanced molecular equation Split electrolytes to their corresponding ions to achieve…

Q: 17 ČH2CECH A CHz CEC CHz

A: Reagents are the chemicals that we add to bring about a specific change to an organic molecule. Any…

Q: BY BY2, hD NOOH Cae) ( Cyclopentane) SM2 он pcC, THE BY BY2 ACOH t'Buok JEBuott E2 Reoction ( dip -…

A: In the first step bromination takes place in presence of sunlight with the production of free…

Q: The order from most reactive to least reactive with aqueous ammonia is (А) CH--o-č-CH, *…

A: The given molecules are acetyl chloride , acetic anhydride,ester molecules.

Q: DRAW: (IR25,3R,4R, GR)- l6-Bromo- 4-tert buby )-3- i5opropyl-2-nitro -1-cyclohexanal- Also s how as…

Q: Draw the structure(s) of the major organic product(s) of the following reaction. H,PO2 CH3

A: In the first reaction, the diazonium salt is reacting with H3PO2 and in the second reaction an amine…

Q: Alkene Z or E?

Q: (CH2 Kuli DNOOHA 2) Atdal condonaten of From fragments of 4 carbons or fewer 3) HoD

A: Aldol condensation is the condensation between two carbonyl compounds to give a β-hydroxy carbonyl…

Q: (a) Br2 FeBr3 (b) NaCN CI (c) HO H,SO, 180 °C Major product

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

Q: 1. %3D CH;CH2CH2-Ĉ-CH2CH3 2. CH3CH2-C-H

Q: 4. A student was asked to prepare an alkene X in high yield using any alcohol as starting material…

A: Since you have asked multiple questions, we will solve the first question for you. If you want any…

Q: Circle the "isoprene" units in the following terpene. Label the head (h) and tail (1) of each…

Q: Q1\ Complete the following reaction by appropriate compounds? H* OH + ? 0-CH3 -NO2 ? -CI

A: ->In acidic medium carboxylic acid react with alcohol and form ester. ->HNO3/H2SO4 used for…

Q: The preparation of CH3-CH2-CH2- NH2 from CH3-CH2-Br could be achieved by using: O NACN then LİAIH4…

A: The product to be produced is a primary amine CH3-CH2-CH2-NH2 forming from CH3-CH2-Br.

Q: Trichloroethylune in puulud 2- slep renehn in Gguenal, a yueld khachlewethane, whih is fost…

A: Given: Standard heat of reaction 1, ΔHr1= -385.75 kJ Standard heat of formation of trichloroethylene…

Q: Does this rechion go mottly Aaur the mechaniam bading to a major orginie quodunt Draw the machamiam…

Q: NEG H2SO4 CF3 SO3 Mono-substitution product OTs K H3C Et THF, 25 °C EIONA EtOH, 80 °C Br

A: The above given a set of reactions. A particular set of reaction leasds to the formation of specific…

Q: 1. sodamide, NaNH2 2. formaldehyde, HCHO 3. Нзо" -%1-hеptanol, CHз(СHг):СH2ОН Е. ? (name, str) -4.…

Q: (Brew the Shuctrie of eadh as -1-ethyl-4- methylaydsherane 5. 2,3-dimethyl-4-propylnomane…

A: The systematic structure determination of organic compound is given by IUPAC. The naming of organic…

Q: The moleculc 2-butcne is able alkenc to a trans-alkene. This t H H.

A: According to the question, molecule 2-butene is able to undergo a process called cis-trans…

Q: y wysthers oy # Wite he mechanisn 1-ocehly/-2-cy clehexen-1-d apududdo Umpeding ghenemuas

Q: 1,3-dichloro 2-mctuyl cycionexanc 6-Chloro -s-ernyi decane mcloheptane Br 1-flu

Q: Name the folowing ?? CH3 CH -CH2-c Hz-CH- CH CH3 CH3 CH3 2(CH), CH-clth-cHz-cHs cH3 CH3-CH-CH-CH3 3.

Q: conc. H,SO, c) -OH A

Q: 2. Draw the reactantls) CH3(CH2)24 C-o-CH2 CCH2)48 CH3 t HzO insect wax

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

Q: Some chemical transformations of alkene A are given in Scheme 1. CH,CH,ONa в ELOH A D K,Cr,0/Acid OH…

A: Different reagents show different reactions, in this scheme alkene converts into epoxide, alkane,…

Q: which af them More Stable isit stable is it more Stable2 and why? why ? 4-hydroxg Pyrid Pne 4-…

A: As the repulsion forces are less, the stability of the compound will be more.

Q: 7. a. Which categories/classes does this compound belong to (for example, aldehyde, ketone)? b. Use…

A: First belongs to thiol family. Second belongs to ketone family .

Q: SoNtion :- (1) (3 10 Br (2 1o membir long Carbon chain So, name is 1- bromo-5-chloro evo -5-cthyl -…

A: To write the name of organic compounds we follow some rules ; Select longest carbon chain or ring…

Q: 4) Which of the following statement(s) is (are) FALSE? a. The alkene below can be named as:…

A: When two same substituents are in same sides i.e. cis orientation, then it is called Z isomer. When…

Q: फोण्ड मैकट वकडुण्सर नoीन्ण्माल वड क्रचe नr विंडल false amd Explaim your gmswer ?ņ (i Alglic…

Q: tehich of Ahe followsng has the Jorrgest mumber of n कटपक कड ?हतविल C1) phoseho80u S-30 xp laim (1)…

A: Atomic number = number of proton Number of proton = Number of electron Number of neutron = mass…

Q: a. Thus, it w Now, the dienophile Although the dienophile has a fancy name it is simply a(n): be…

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

Q: 3CH2CH2CH2C(CH3)2 a this alcohol be synthesized selectively by hydrobor If yes, draw the structure…

A: In Hydroboration-Oxidation Reaction anti-markonikov rule follow. Anti-markonikov rule says that…

Q: What is the correct structural formula for C4H8O which is "carbocyclic"? Select one: Oa. O b. HO.…

Question

Answer Nos. 7-12 Only.

Write only the product and the type of reaction it undergone.

Thank you!

A t and write the UPAC name of the Major Organic Produa fomed
ALCOHOLS & ETHERS
by e foowng reactions
1 entene• H0 H50.
CH
2 CHICHCH,MgCI + CH,CHCHO –M,0
1 schioropropane + Sodium hydroxide
. CH,CH;CH,CH,COOH • LIAIH, ether
5. CH,CH,MGCI + HCHO0
CH
6 CH,CH;CCH, + CH;C-M9CIH0
7. Chioroethane + CH;ONa
8. Ethane + water _H,50.
mondon
2 CH,CH;CCH,
10. 2moles of 1-propanol 140°C
LIAIH, ether
11. CH.CHCH;CHO
CH,
+ LIAIH._ether
12 CH,CH,C-OCH;CH,CH, + LiAIHe_ether

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 3

VIEW

Step by step

Solved in 3 steps

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

Types of Polymers on the Basis of Physical Properties

Learn more about

Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.

Similar questions

I’m currently trying to write a lab report for the synthesis of dimolybdenum tetraacetate [Mo2(O2CCH3)4] from the reaction of molybdenum hexacarbonyl, Mo(CO)6 in glacial acetic acid and acetic anhydride under a nitrogen atmosphere, involving the difficult formation of a quadruple bond and requires high heat and long reaction time (approximately 20 hours). But these are the question I’m stumped on: 1. Why need the reaction be done under nitrogen? We also added dichlorobenzene and hexanes during the reaction. 2. Explain the purpose of dichlorobenzene and hexanes. 3. Why does the reaction take 20 hrs?
Pls solve this question correctly in 5 min i will give u like for sure Balance the chemical equation of a reaction formed by the bromination of trans-cinnamic acid if we started with 0.3088 grams of trans cinnamic acid and 1mL of bromine. The product of this reaction is 2,3 - dibromo - 3- phenylpropanoic acid
Oxidation of Butanol -1 in KMnO4/H+ will produce-------------. a.Butanoic Acid b.Butanal c.Pentanoic acid d.Butene -2
what is the best way to come up with how to synthesize carboxylic acid , oct-4-yne to butanoic acid, or trans cyclodecene to decanedoic acid . I keep getting confused on how to go from the reactants to product, even with the amines. i can't figure out what to use to get to the product. Please explain Grignard rx as well.
KMnO4, warm, conc'd reacts with hept-1-ene to yield __________. CO2, hex-1-ene CO2, hexanoic acid Formic acid, pentanoic acid Ethanoic acid, pentanal Formic acid, hexanone
Can some one help to explain this slide? In hydration of alkenes, Is hyohoboration always give a non-Markovonikov product? Is oxymercuration always give a Markovonikov product? In syntheisis of diols, Is hydroxylation always give a Cis 1,2 diol? Is mCPBA (meta-chloroperoxybenzoic acid) always give a tran 1,2-diol? Pleease give backgound informations, and details to support the explanation. (Please draw the Mechanism to help me understand the principle if you can)
A chemist allows some pure (2S,3R)-3-bromo-2,3-diphenylpentane to react with a solution of sodium ethoxide(NaOCH2CH3) in ethanol. The products are two alkenes: A (cis-trans mixture) and B, a single pure isomer. Under thesame conditions, the reaction of (2S,3S)-3-bromo-2,3-diphenylpentane gives two alkenes, A (cis-trans mixture) and C.Upon catalytic hydrogenation, all three of these alkenes (A, B, and C) give 2,3-diphenylpentane. Determine the structuresof A, B, and C; give equations for their formation; and explain the stereospecificity of these reactions
Predict the major products formed when 2- methyl-1-butene reacts with: H2, Pt/25°C. Show the reaction mechanism the given alkene reactions
QUESTION 10Suggest the synthetic sequences including reagent(s) and condition for the preparation of the following compounds:a) 3-heptyne from ethyneb) Octyne from ethynec) CH3CH2CH(CH3)CH2COCH3 as major product from suitable alkyned) 3-octyne from butynee) CH3CHO from ethynef) 1,1-dibromo-4-methylhexane from suitable alkyne
Acid-catalyzed hydrolysis of a nitrile to give a carboxylic acid occurs by initial protonation of the nitrogen atom, followed by nucleophilic addition of water. Review the mechanism of base-catalyzed nitrile hydrolysis in Section 20-7 and then predict the products for each reaction below and write all of the steps involved in the acid-catalyzed reaction, using curved arrows to represent electron flow in each step.
E. J. Coreys 1964 total synthesis of -caryophyllene (essence of cloves) solves a number of problems of construction of unusual-sized rings. The first step uses an efficient photochemical [2 + 2] reaction. The desired stereochemistry and regiochemistry had been predicted based on model reactions. (a) [2 + 2] Reactions are quite common in photochemical reactions. Would this reaction be predicted to occur in the ground state? The next steps follow. Basic alumina is a chromatography support that will often act as a base catalyst. (b) What is the mechanism of the first step? (c) What is the mechanism of the second step? (d) Look at later steps in the synthesis. Does the stereochemistry of the added carbomethoxy group matter? The next steps are shown here. (e) What is the structure of compound (A)? (f) Give a mechanism for the formation of the cyclized product. (g) Give a mechanism for the first step. Hint: Attack on the lactone carbonyl may be the first step. (h) Give a structure for product (B). The following two steps are next. (i) Show the reactions of (B). (j) Write a mechanism for the ring-opening reaction. Hint: Note the presence of an acidic proton and a good leaving group in the molecule. The synthesis was completed by the following steps. (k) What is (C)? (l) What reagents would you use for these transformations?
Does the data provide evidence for the claim that the reaction of Br2 with alkenes proceeds via anti‐addition? YES OR NOW AND WHY The mleting point of the product was found to be 234.5-235.5C chemical reaction: trans-stilbene+pyrimindine tribromide --->acetic acid 1,2-di bromo-1,2-diphenylethane product was trans-1,2-dibromo-1,2-diphenylethane