Question 1 1 pts How many unique products (including regioisomers and stereoisomers) could be produced with the molecule shown below is heated in ethanol? Assume no rearrangements will occur. ELOH 0 1 O 2 O4 O 5
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Q: QUESTION 8 What is the major product of the following reaction? 앙ㅇ CHCH₂ OH
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Q: 1. ВНя/THF 2. H2О2/NaOH
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- C10T05Q3420 Give the major organic product for the following reaction. H H H catalytic heat if There is no reaction under these conditions or the correct product is not listed here.esc 1 O PRINCIPLES OF ORGANIC CHEMISTRY Classifying organic reactions The following chemical equation is for an elimination reaction, where the important atoms, groups, and bonds involved have been highlighted for you: Explanation O. -H 2 Use the information provided to predict the missing organic product and draw its structure in the drawing area below. Make sure to use the same skeletal ("line") style for the structure as the rest of the equation. Check H* Click and drag to start drawing a structure. w # 3 Q + H-0 $ 4 % 5 6 MacBook Pro & 7 Draw or edit atoms, groups, or bonds X C * 00 2/5 Cx 8 + Kimberly V © 2023 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility ? olo Ar + 1 HARHow many unique products (including regioisomers and stereoisomers) could be produced with the molecule shown below is heated in ethanol? Assume no rearrangements will occur. ..CI ELOH O 1 2 4 O 5
- s 2req 2req 2req 2req 2req Visited Complete the equation for the following reaction by drawing a structural formula for the missing organic product. Onomorecom NH3 CH₂ + You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. • Draw cations and anions in separate sketchers. Ⓒ%81 CH₂ H₂O ? Y Jn [1It is a type of organic reaction in which parts from two molecules exchange. * Elimination Substitution Addition Rearrangement In the reaction given below, what type of addition reaction is used? * H H H H H-C-c=C HBr н-с — с — С —с —н + H H H Br H O Hydrogenation O Hydrohalogenation O Halogenation O Dehalogenation H-O-I888 4 [Review Topics] [References] Draw the structure(s) of the major organic product(s) of the following reaction. i 5 O C % T HO • You do not have to consider stereochemistry. • If a compound is formed more than once, add another sketcher and draw it again. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right e F5 corner. . Separate multiple products using the + sign from the drop-down menu. JUL 9 OH 6 98 1 [*** Y Br // 0 F6 H ChemDoodleⓇ MacBook Air & tv 7 F7 U * dry HCI cold 00 8 Sn [F C DII FB I ( 9 K ла DD F9 O ) O L & W F10 P a (1 F11 { + "1 = ? Previous F12 1 Next> Save a del
- The reaction of 3-methylene-1-cyclohexene and HBr yields the four products shown in the attachment. Which two are formed at high temperatures and which two are formed at low temperatures? Why? Why is 1-bromo-3-methylenecyclohexane not formed?For the reaction shown below, draw the structure(s) of the major product(s) expected. Do not draw duplicate structures of the same molecule as different products. (Do this on a piece of paper, then scan into PDF file and upload.) H,SO,/SO3 5 deg C CH3Q3. For the following reactions, predict the products, mechanism and name all the products 4.2-hexene + chlorine gas5.Halogenation of cyclohexane in the presence of light and catalyst6.Sulfonation of Cyclobutane with oleum 7.Addition of HBr to methylcyclopropane
- 27. For each example, identify what type of organic compound is present out of the following options: ketone, ether, carboxylic acid, aldehyde, or alcohol. нн нн Н-С-С-О—С-с-н нн нн нон Н-С-с-с—Н H H | Н-с-о-н H エ-O-エ1. Consider the following reaction - Dehydrogenation of Methyl Cyclohexane (MCH) to Toluene (TOL) using a Precious Metal (Pt) supported on Alumina. CH3 CH3 2 () + 3 H₂ Typically, hydrogenation of a cyclo-alkane, like MCH, occurs in 3 or more stages, where one bond is dehydrogenated per stage, eventually resulting in the dehydrogenation of 3 bonds. Strong adsorption of MCH is likely to occur, but the adsorption of hydrogen (either as a molecule on a single site OR as an atom on a single site) is unclear. Therefore, in this question, two types of reaction mechanisms are to be considered, as discussed below: (a) You are to first propose a reaction mechanism which includes adsorption, surface reaction, and desorption. For each of the following cases, please write down a full set of elementary reaction mechanisms. (0) Extraction of Hydrogen in 3 stages, based on dehydrogenation of each bond-where the ensuing hydrogen product is adsorbed as a molecule on a single site, in one step.…CH3 CH3 Br- Br2 .CH3 CH2Cl2 CH3 H3C H3C Br Electrophilic addition of bromine, Brɔ, to alkenes yields a 1,2-dibromoalkane. The reaction proceeds through a cyclic intermediate known as a bromonium ion. The reaction occurs in an anhydrous solvent such as CH,Cl,. In the second step of the reaction, bromide is the nucleophile and attacks at one of the carbons of the bromonium ion to yield the product. Due to steric clashes, the bromide ion always attacks the carbon from the opposite face of the bromonium ion so that a product with anti stereochemistry is formed. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions CH3 CH3 CH3 CH3 H3C H3C :Br: :Br: