Predict the major products of this organic reaction. Be sure you use dash and wedge bonds to show stereochemistry where it's important. + Х OH 1. TsCl, py 2. Na Br
Q: Determine the isomeric relationships between the following compounds. The possible relationships are…
A: You can see accurate relationship in the last image . Explanation is also given on remaining pages,…
Q: Fill in the missing boxes for the reactions below. a. 1) O3, -78°C 2) Zn, CH3COOH + b. 1) Of 2) Zn,…
A: Step 1: Step 2: Step 3: Step 4:
Q: Predict the product of propanoyl chloride reacts with the reagents listed.
A:
Q: Identifying the enantiomer of a simple organic molecule Check the box under each structure in the…
A: Enantiomers:The non-superimposable mirror image forms of chiral molecules are called enantiomers. We…
Q: 8.37 The diatomic cations Br₂+ and 12+ are both known. a. On the basis of the molecular orbital…
A: In conclusion- The changing in color is based on the energy increasing between LUMO and HOMO. -…
Q: Give me detailed mechanism Solution with explanation needed. don't give Ai generated solution. avoid…
A:
Q: Please correct answer and don't use hand raiting
A: Step 1: Step 2: Step 3: Step 4:
Q: After studying your printed calibration graph, answer the following questions. a. Which variable is…
A: a. Dependent Variable is plotted on the y-axis (note: photo of the calibration graph is blurred, the…
Q: Calculate the pH of a solution prepare by mixing 5.97 mL of 0.107 M NH3 with 10.10 mL of 0.0286 M…
A: First, we need to calculate the number of moles of NH3 and HCl. The number of moles can be…
Q: where are the chiral centers on a ritonavir molecule
A: Approach to solving the question:A chiral center is a carbon center that has four different atoms…
Q: Propose a structure for the carboxylic acid, C7H14O2, with the following 13C and DEPT NMR data:…
A:
Q: ja.1
A: The structure of cis-1-ethyl-2-methylcyclohexane can be drawn by first drawing a cyclohexane ring,…
Q: Use this to show [OH] x [H+] = 10-14
A: Step 1:Equilibrium expression for the ionization of water:H₂O(l) ⇌ H⁺(aq) + OH⁻(aq) Equilibrium…
Q: arning achieve.macmillanlearning.com Chapter 6 HW - General, Organic, and Biological Chemistry for…
A: D-fructose is a hexose sugar with the chemical formula C6H12O6. It has a ketone group on the second…
Q: Give the IUPAC name for the following compound: H CH2CH3 CH2CH2CH3 H3CH2CH2CH2C CH2CH3 CH2CH3
A: At first draw the molecule in sawhorse projection from Newman to understand the two carbons we…
Q: Don't use AI.
A: Approach to solving the question: As we know, the stability of carbocations are given as,3° > 2°…
Q: Please correct answer and don't use hand rating
A: The pH at the equivalence point (when 25.00 mL of HCl is added) is 5.41. This is crucial for…
Q: O Macmillan Learning Chapter 6 HW - General, Organic, and Biological Chemistry for Health Scien…
A: The substance that is not digestible by humans is cellulose. Cellulose is a complex carbohydrate, or…
Q: Show work with explanation needed. don't give Ai generated solution
A: Step 1:Solution:Given three acid-base reactions.1):…
Q: © Macmillan Learning gane Sc Resources Per Draw an alcohol with the formula C5H12O that contains one…
A: An alcohol with the molecular formula C5H12OH with a chiral center is Pentan-2-ol. The chiral center…
Q: Draw all possible elimination products for the reaction below. NaOH 1/20 n. ?
A:
Q: Listed below are several hypothetical nucleophilic substitution reactions. None is synthetically…
A: Approach to solving the question: B- The formation of H- is highly unfavorable as the negative…
Q: Calculate the pH of a solution obtained by mixing equal volumes (1 mL each) of 0.101 M H2SO4 and…
A: First, we need to identify the reaction that occurs when H2SO4 and NaOH are mixed. H2SO4 is a strong…
Q: Please correct answer and don't use hand rating
A: Step 1: ReactionAbove reaction is an elimination reaction and it involves E2 mechanism.8 M NaOH is…
Q: Imagine that you analyzed the original distillation mixture from Exp #3 using a Gas Chromatography…
A: Step 1:Final Answer:You are required to combine all these aspects (FID signal with retention times,…
Q: Predict the major products of the following reaction. Be sure to use wedge and dash bonds to show…
A:
Q: Show work with explanation needed...don't give Ai generated solution
A: Step 1: For naming this compound, you just need to first catch the parent chain or in other words…
Q: Convert a pressure of 1365 torr to atm.
A: In order to convert pressure from torr to atmospheres (atm), we need to know the conversion factor…
Q: Show work. Don't give Ai generated solution
A: pka value:pka is negative log of acid dissociation constant (ka). pka is inversely proportional to…
Q: help please answer in text form with proper workings and explanation for each and every part and…
A: Thermodynamics work (W) is equal to changes in volume at constant pressure, such as in a piston.W =…
Q: [References] Draw the products of the following reactions, indicating both regiochemistry and…
A: Step 1: Step 2:Mechanism Step 3: Step 4:
Q: Please correct answer and don't used hand raiting
A: Step 1: Redox ReactionReaction in which oxidation and reduction occur simultaneously is known as…
Q: Disaccharides Disaccharides are carbohydrates composed of two monosaccharide units that are joined…
A: 1. Identify the Disaccharide LinkageIn the structures of maltose, lactose, and sucrose provided in…
Q: The buffer mentioned in the image is from the following question:"What is the pH of a buffer made by…
A: The pH of buffer solution calculation:Step 1:The buffer prepared from weak acid and their conjugate…
Q: Please correct answer and don't use hand raiting
A: Step 1:To keep the temperature from changing, the heat absorbed or released by dissolving one…
Q: Experiment for Kinetics – The Iodine Clock Reaction Results A1: Trial 1: took 43.64 seconds to turn…
A: Average times:A1: (43.64 + 44.82 + 47.49 + 45.23 + 43.63) / 5 = 44.96 s A2: (55.10 + 52.77 + 44.67 +…
Q: Don't use AI.
A: A)In elimination reactions, regioselectivity and stereoselectivity refer to different aspects of the…
Q: 33. NO AI USE
A: Step 1: 1H NMR1H NMR (proton nuclear magnetic resonance spectroscopy) is a powerful analytical…
Q: Bookmarks Window Help achieve.macmillanlearning.com Macmillan Learning tion 7 of 32 > tv $ ©…
A: In chemistry, an alcohol is an organic compound in which the hydroxyl functional group (-OH) is…
Q: Provide a balanced NET IONIC EQUATION, if applicable, for every reaction below. If no reaction…
A: Step 1: Write the…
Q: What are wrong with the reagent and how can it be fixed.
A:
Q: provide the organic structures and reagents that effieciently produce the target products the…
A: Step 1: Step 2: Step 3: Step 4:
Q: Please correct answer and don't use hand raiting and don't use Ai solution
A: Part A:Using the ideal gas…
Q: Enter electrons as e¯. Use smallest possible integer coefficients. If a box is not needed, leave it…
A: Step 1: Step 2: Step 3: Step 4:
Q: trans-1-ethyl-2-methylcyclohexane Drag the appropriate labels to their respective targets. Note: not…
A: Approach to solving the question:Here we just need to connect the given substituents according to…
Q: A student was given an unknown metal. The student determined that the mass of the metal was 30.2 g.…
A: Step 1: GivenMass of the metal = 30.2 g Initial volume of water = 20.0 mL Final volume of water with…
Q: It is important to always minimize the amount of solvent used, allowing for evaporation. If we add a…
A:
Q: Fill in what's missing in the box for the reaction below
A: Step 1: Alkenes and alkynes can undergo oxidative cleavage with ozone (O3) to give carbonyl…
Q: Please correct answer and don't use hand raiting
A: The problem involves analyzing the molecular orbitals (MOs) of trimethylenemethane, a molecule with…
Q: Show work. Don't give Ai generated solution
A: Final Answer with Explanation:Arrangement of Substances Based on Acid Strength:Strongest acid:…
Step by step
Solved in 2 steps with 1 images
- Predict the major products of this organic reaction. Be sure you use dash and wedge bonds to show stereochemistry where it's important. XOR OH 1. Ts Cl, py 2.t-Buo k Click and drag to start drawing a structure.5.Synthesis. Make the following products from a suitable cyclic alkene starting material. Look at the functional group PATTERN present in the molecule, including stereochemistry. Br CH 3 Br CH3Predict the major products of both organic reactions. Be sure to use wedge and dash bonds to show the stereochemistry of the products when it's important, for example to distinguish between two different major products. + X H₂O Click and drag to start drawing a structure. + © A B 1. Hg (OAc)2, H₂O Click and drag to start drawing a structure. 2. NaBH4
- Draw a structural formula for the major product of the reaction shown. Br2 =CHCH2CH3 H20 • Show product stereochemistry IF the reactant alkene has both carbons of the double bond within a ring. • Do not show stereochemistry in other cases. • If the reaction produces a racemic mixture, just draw one stereoisomer. aste ChemDoodle Previous Next Save and Exi tv MacBook Air DD 80 888 F11 F12 F9 F10 F7 F8 F5 F6 F3 F4 & ( ) #3 $ % %3D 3 4 6 7 8 9. { } P E Y U D G H J K F > .. .. RPredict the major products of both organic reactions. Be sure to use wedge and dash bonds to show the stereochemistry of the products when it's important, for example to distinguish between two different major products. ab Pck Check + Х 80 F4 14 C 1. R₂BH 2. H₂O₂, NaOH '2 2' Click and drag to start drawing a structure. % 205 F6 07 & E 18 Ar B Save For Later Submit Assignment © 2024 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility A F7 E W R T Y U S D F G H * 00 8 A A» Fa FO F10 F11 F12 Ο O P { J K L Z X C V B N M 1- H A option command H > ? command optionPredict the major products of this organic reaction. Be sure you use wedge and dash bonds when necessary, for example to distinguish between major products with different stereochemistry. : ☐ + Х RCO₂H 3 Click and drag to start drawing a structure.
- What is/are the major product(s) of this reaction se 1. ВНЗ 2. H2O2, NaOH 3. PBR3 4. (CH3)3COK/(CH3)3COH +1Predict the major products of this organic reaction. Be sure you use dash and wedge bonds to show stereochemistry where it's important. OH : + ☑ G 1. TsCl, py 2. NaSCH 3 Click and drag to start drawing a structure. 00 مله ArPredict the major products of both organic reactions. Be sure to use wedge and dash bonds to show the stereochemistry of the products when it's important, for example to distinguish between two different major products.
- Predict the products of this organic reaction: CH3 O || CH3 CH–C−NH—CH3 + NaOH A No Reaction ? Specifically, in the drawing area below draw the structure of the product, or products, of this reaction. If there's more than one product, draw them in any arrangement you like, so long as they aren't touching. If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area. Click anywhere to draw the first atom of your structure. X :0 Ć1. Assign E or Z to the following alkenes. If the alkene does not have stereochemistry, write "NONE". H CI H3C SH T. H CI, ОН H3CH2C НО D D EN C(CH3)3 CH3 Me H Et N' 'N' C=C H3C Et Me what Columbus sought in the 'Indies' - Piperine CH2OH Br (H3C);C, H3C HOH, CH,CF, H3C Br HOH2C НО H the spice Columbus found (Capsaicin) HO. Muscalure Bombykol (the sex attaractant for the male silkworm) (the sex attaractant for the common housefly) OH .CO2H the "heart healthy" part of olive oil a 'less healthy' trans fatty acid from trans fatCH3 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: