QUESTION structure of the final products A and B. Provide a complete mechanism with arrow pushing The two reactions below give slightly different products. Show the showing the intermediates and all resonance forms for one transformation. Explain the differences between the two reactions. HCI (cat) CH2CH3 CH3OH (excess) Зда HCI (cat) B CH2CH3 CH CH2OH (excess)
Q: slove part c
A: Sure, The temperature rise, standard molar enthalpy of formation, and C-C bond dissociation energy…
Q: Please don't provide handwritten solution.
A:
Q: Indicate the name of the compound in the figure and indicate how it is obtained from 1-(3-…
A: Sure, I can help you with the question based on the image you sent.The question asks you to identify…
Q: Be sure to answer all parts. Complete the reactions to show how the following product can be…
A:
Q: None
A: a. ΔS(surroundings)=0According to the second law of thermodynamics, for any spontaneous process, the…
Q: Problems: 1. Predict the product and show the mechanism for the following intramolecular reaction. H…
A: This reaction is completed in four steps of the reaction mechanism. Step 1: In the first step, the…
Q: 1. Predict the product and show the mechanism for the following intramolecular reaction. H H cat.…
A: This reaction is completed in four steps of the reaction mechanism. Step 1: In the first step, the…
Q: Draw the product of the following epoxide reaction, including the stereochemistry at any stereogenic…
A:
Q: None
A: Step 1:The most common ions of aluminum and sulfur are:Aluminum (Al): Al3+ (aluminum cation with a…
Q: 18. What is the third intermediate of the following reaction? R shown.) R a. R. b. R 6-0-0- -0-0-6 R…
A: The process to identify the correct intermediate step-by-step involves understanding the mechanism…
Q: /&:$;$;):)):):$:$:$
A:
Q: 2. Suggest two sets of conditions that would be needed to form the following cyclic ester (called a…
A: the mechanisms for the formation of tetrahydro-2H-pyran-2-one (lactone) from ethyl…
Q: An arctic weather balloon is filled with 40.3 L of helium gas inside a prep shed. The temperature…
A: Approach to solving the question:Please see attached photos for detailed solutions. Thank you.…
Q: Explain the difference between dilute and concentrated solutions.
A: First let's understand solution. Solution is a homogeneous mixture that generally contain two parts…
Q: None
A: In case of any doubt please feel free to ask.
Q: In which of the following alkenes will a hydride shift occur upon adding HCI ? a. 0 O b. c. d. e.…
A: All the alkene structures shown (a, b, c, and d) are simple non-cyclic alkenes without any…
Q: 16) What is the major product of the following reaction? N NH . Br Br Br Br L IV. N :NH N. :NH II.…
A: Step 1: Step 2: Step 3: Step 4:
Q: Answer the questions in the table below about this molecule:
A: Detailed explanation:Identification of the Molecular Structure: The molecule presented,…
Q: None
A: Approach to solving the question:By definition, ketohexoses are a class of carbohydrates that have 6…
Q: Please show the major products with appropriate stereochemistry where needed.
A: Step 1:• Mechanism: • Aniline react with NaNO2 to give diazobenze.• diazobenzene react with…
Q: Draw the major product of this reaction. Ignore inorganic byproducts.
A: Step 1: Step 2: Step 3: The Michael addition reaction is nucleophilic addition to unsaturated…
Q: H₂O N(CH3)2 H₂SO a. Draw the structure of the tetrahedral intermediate INITIALLY-FORMED in the…
A: In case of any doubt please feel free to ask.
Q: 1. Establish the symmetries of the resulting many-electron states. To do that, you will use the…
A: Approach to solving the question & Detailed explanation:Understand Symmetry Operations:Review…
Q: Solution for the uploaded question please.
A: Step 1:Step 2:Step 3:
Q: Which of the following statements about helium, neon, and argon is true? Question 11 options:…
A: They have the same number of protons.Helium has 2 protons, neon has 10 protons, and argon has 18…
Q: Use retrosynthesis Mecanism use TCCA . Dont use PCcA
A: Step 1: Step 2: Step 3: Step 4:
Q: Write the Equilibrium Expression for each of the three reactions below 1) CH4(g) + 2O2(g) →…
A: Step 1: Step 2: Step 3: Step 4:
Q: Please don't provide handwritten solution.
A: Step 1: Step 2: Step 3: Step 4:
Q: 1. Draw a diagram to show how two ethanol molecules can H-bond with the soap molecule. O ||…
A:
Q: Answer asap
A: a. Description of the Method for Determining the Rate of PhotosynthesisThe botanist can determine…
Q: What are the products of the following reaction? 우- он CH₂OH OH CH, CH₂OH OH OH CH₂OCH2CH3 OCH2CH3…
A: Step 1: Step 2: Step 3: Step 4:
Q: Label and describe all the components of a polarogram.
A: These components work together to generate a polarogram, which provides valuable information about…
Q: What is the major product of the following reaction? Br N Br NaOCH 3
A:
Q: 3 ✓ 14 ✓ 15 ✓ 16 ✓ 17 ✓ 18 19 20 21 ✓ 22 ✓ 23 III Review Homework REQUIRED (NOT Pie Progress)…
A: Step 1: We know that, q=mCdT T2=16.1+273=289.1KT1=−0.6+273=272.4K =>q=mC(T2−T1)…
Q: Change Add water Add oxygen Lower the temperature Raise the temperature Decrease the pressure 2H2(g)…
A: Step 1:Given reactions,1st ) exothermic , having more moles of Gas at reactant side 2nd )…
Q: Look at the titration curve below and determine what acid from the list could be the acid being…
A: Step 1: Determine the volume at the equivalence point. From the given titration curve the volume at…
Q: Prepare the compound by using suitable reagents. More than one step will likely be required.
A: To synthesize 4-(6-methoxynaphthalen-2-yl)butan-2-one from acetoacetic ester, we can use a multistep…
Q: Please correct answer and don't use hend raiting
A:
Q: QUESTION 4 your choice. .ank the following compounds below In terms of acidity and explain CF3CH2OH…
A: Step 1: We know, According to Bronsted-Lowry acid-base theory, an Acid is a H+ donor whereas a Base…
Q: Predict the structure of the alkene you would use to prepare the alkyl halide below. Br (only…
A: In case of any doubt please feel free to ask.
Q: What is the enthalpy of combustion of (in kJ) of a couch weighing 60 lbs? 1) Do not use scientific…
A: Step 1: Convert the mass of the couch from pounds (lbs) to grams (g). The conversion factor between…
Q: nem NH2
A: Step 1: Step 2: Step 3: Step 4:
Q: 3) Given the following reaction: a) Draw the mechanism for the formation of two possible compounds,…
A: The reaction mechanism for the formation of two possible compounds, which are isomers, can be…
Q: dont provide handwriting solution....
A: The portions of 1,2,3-Trichloropropane that interact differentially with water molecules are…
Q: Argue that the below structure is D-galactopyranose. This is most easily done with a drawing. OH HO…
A: Step 1: key features of D-Galactopyranose Step 2:identification Step 3: structure understanding…
Q: None
A: Step 1: Information: These questions depends on protection and deprotection of compound . The answer…
Q: The compound G's 1H-NMR spectrum is shown below. Assign the spectrum (feel free to just use arrows…
A: For the 1H-NMR Spectrum:For the peak at around 1.27 ppm these hydrogens are the most shielded.…
Q: Calculate the expected mass of calcium sulfate: Na2SO4 + CaCl2 -> CaSO4 + 2 NaCl 142 g (Molar Mass)…
A: since data of reactant is not given let me give you brief idea assuming you have data. Na2SO4 +…
Q: Question 7 (2 points) According to the chemist system, what is the correct carbon designation for…
A: Carbon Number Assignment of Fatty AcidsFatty acid carbon atoms are numbered starting at the terminal…
Q: Macmillan Learning Consider the reaction. I CH3 3 NaOH CH3 What are the fatty acid products of the…
A: Saponification is the process in which triglycerides are combined with a strong base to form fatty…
Step by step
Solved in 2 steps
- The diol shown undergoes reactions with reducing and oxidizing agents to yield two different products: A and B. Draw the major organic product for each of the reactions shown. ОН of ОН (A) Reaction with MnO, in propanone at 25 °C. (B) Reaction with KMNO,, HO¯ and heat, followed by 4> an acidic aqueous workup. Select Draw Rings More Erase Select Draw Rings More Erase H C HIdentify the reactions needed to prepare A) (1) Acetyl chloride, (2) LIAIH4, (3) Benzyl bromide B) (1) Benzaldehyde/NaBH3CN, (2) Formaldehyde/ NaBH3CN C) (1) Methyl iodide, (2) Acetyl chloride, (3) LIA|H4 D) (1) Benzyl bromide, (2) NaBH3CN N-benzyl-N-methylbutylamine from 1-aminobutane?(i) H₂C (ii) (iii) H₂C (iv) (v) a. Draw the missing Reactant or Product for each of the following reactions. OH OH H*/KMnO4 H₂SO4 HCI H* / CH₂OH H* / K₂Cr₂O₂ H₂C Product A H₂C. H₂C CI CH 3 CH 3
- Draw a structural formula for the major organic product of each reaction and specify the most likely mechanism by which each is formed. (g) CH3CH2ONa++CH2=CHCH2ClethanolQuestion: Which reaction would be the best synthesis of the following compound? CH3-CH- NH- CH2- CH3 CH3 (a) (b) EtOH CH3-CH-Br + CH3-CH2- NH2 EtOH CH3-CH=CH2 + CH3-CH2- NH2 CH3 (c) (d) EtOH EtOH CH3-CH-Br + CH3-CEN CH3- CH-NH, + CH3-CHy- Br CH3 CH3 (A) (В) (D) Question: What is the IUPAC name for (СН3)3ССН(ОН)CH2CH(OH)CH2CH(C НЗ)2? * 1,1,1,6-tetramethyl-2,4-heptanediol 2,2,7-trimethyl-3,5-octanediol 2,2,6,6-tetramethyl-3,5-heptanediol 2,7,7-trimethyl-4,6-octanediol O O2. Suggest a stepwise synthesis for the following reactions. CLEARLY showing the PRODUCTS AT EACH STEP. NOTE: Only indicate the product(s) at each step. No Mechanism required for this question! a) -OCH2CH3 from -OH + CH3CH2OH from b) Br from
- Complete the Reaction below and provide the following (i) a detailed stepwise mechanism to account for the product(s), including all steps involved (ii) Clearly show all the resonance structures and intermediates formed leading to the product. OH acetic anhydrideQ16. What are the necessary reagents to perform the following synthesis? Choose the answer from the options below. DG (0) CH3MgBr/ether (1) NaBH4, (2) H3O*(aq) c) H₂, Pt d) (1) CH3MgBr/ether, (2) H3O*(aq) (ii) dilute HCl(aq) conc. H₂SO4(aq) conc. H₂SO4(aq) conc. H₂SO4(aq)A chemist needs an ether to use as a solvent for a reaction and wants to synthesize it in one step from two of the following available reagents: sodium ethoxide, bromomethane, potassium tert-butoxide, and 2-bromo-2-methylpropane. i) Which combination(s) will give a good yield of an ether? Illustrate, showing the mechanism of the reaction. ii) Illustrate with a mechanism the reaction of one of the combinations that will not yield an ether?
- 1) 2) Please give a detailed stepwise mechanism for the following reactions. All arrows, charges, and intermediates must be shown. NaOH, H2O, heat i CHÍNH, + N CH3OH Hg) Arrange the following acylating reagents in terms of increasing reactivity. Discuss your choices. `NH -NO 2 `NH `NH. i ii i h) Arrange the following acylating reagents in terms of decreasing reactivity. Discuss you choices comprehensively. H3C O. F3C H3C (а) (b) (c) i) Which strategy is used in the following reaction to prevent alcohol formation? Motivate. OCH 3 Na H2C- (after H 0*workup)Devise synthetic routes that allow you to get from the reactant/starting material side of the reactions to the product side. More than one transformation may be needed in each case. (a) H3C₂ (b) OH mayon H3C₂ OH ? ? H3C₂ H3C OH SH