2A. Provide a mechanism for the following reaction. 2B. Fill in the bubbles consistent with the order of reactivity you chose. 2C. Calculate the Keq for your acid base step. (pKa R₂NH = 35, RNH = 10) 2D. Add the appropriate wedge/dash to the methyl group in the product. 2D. Add appropriate wedge/dash to Me. 2A. Add curved arrows. Br H H + NMе3 Me N H + Br +HNMе3 2B. Step 1 O acid/base OSN2 O acid/base 2C. Calculate the Keq for Step 2 OSN2 your acid/base step: 10^ Page 1 of 1
Q: Fill in the boxes with the product of the following reactions of alkenes. Draw only the PREDOMINANT…
A: Alkene reacts with hydrohaloacid or H2O/ H2SO4 gives gives alkyl halide and alcohol respectively.
Q: predict the product
A: The objective of the question is to predict the product of a series of chemical reactions involving…
Q: 6. How many moles of iron metal are produced when 3.2 mol iron (III) oxide and 2.3 Fe2O3 + 3CO2Fe…
A: When one or more chemical species react with each other then one or more products can can be…
Q: 0 H 1.LIAIH 2. H₂O 3. PB. Pyr ? Major Organic Product 0 0 HO
A:
Q: Nitesh
A: The objective of this question is to calculate the change in Gibbs free energy (ΔG) for a reaction…
Q: At a certain temperature, 0.4611 mol of N2 and 1.561 mol of H2 are placed in a 5.00 L container.…
A:
Q: Q2. 22 (a) Write down the Hamiltonian of a molecule having M nuclei and N electrons with a dear…
A: The Hamiltonian of a molecule having M nuclei and N electrons is given by the following equation: H…
Q: Draw Fischer projections of the two products of the reaction of D-fructose-1,6-bisphosphate…
A: Given reaction is fourth step of glycolysis.Aldolase is glycolytic enzyme used in glycolysis.
Q: Ammonia will decompose into nitrogen and hydrogen at high temperature. An industrial chemist…
A: Here, The reaction is,2NH3 -------> N2 + 3H2Initial concentration of ammonia gas=8.3 mol/25.0 L…
Q: Please don't provide handwritten solution ...
A: Mass percentage of acetaminophen = 1.96 %Molarity of ethanol= 1.34 MExplanation:no of moles =…
Q: H₁₂C HO CH, H.C H.C CH₁₂ CH₂ CH, N о P S L F க
A: Given is one of the step of organic reaction mechanism.The given reaction is acetalisation…
Q: Question 18 For the compound below please choose the correct set of chair and flipped chair…
A: The basic principle is; the bulky group should always come at equatorial position.The higher the…
Q: This compound is an acetal. Truc O-CH3 O-CH2-CH3
A: An acetal is a functional group characterized by a central carbon atom bonded to two alkoxyl groups…
Q: 4.36 Give the lUPAC name for each compound. 9. h. i. ཅན་གྱི་ན་གྱི་རིང་གྱི་ཆ་ག་པའི་་་་་…
A: Note:-“Since you have posted a question with multiple sub parts, we willprovide the solution only to…
Q: How many electrons were used up before placing the lone pairs in sulphuric acid structure? A. 16 B.…
A: Lewis structures, also called Lewis dot diagrams or electron dot structures, are diagrams that…
Q: Select the major product of the following reaction. OH LOH of HIO4 - 5 of of of a Give detailed…
A: Given reactant:So, this is a vicinal diol since it has two OH groups at the two adjacent carbons.
Q: (a) CN 0 0 1. H₂O X, A 2. SOBг2, N 3.(CH3CH2)2CuLi; H₂O 4. NaBH4, CH3OH
A: The question is based on the concept of organic synthesis.We need to synthesize the product using…
Q: A 30.00-mL sample of 0.125 M HCOOH is being titrated with 0.175 M NaOH. What is the pH after 21.4 mL…
A: Molarity is one of the terms to express the concentration of the solution. Molarity is defined as…
Q: Please determine the total mg/mL that you were able to recover from the column= experimental yield.…
A: Optical density (OD) or absorbance is a measure of light absorbed by the light. It can be calculated…
Q: Which molecule is a meso compound and is therefore optically inactive? CI CH3 CH2 CH2 CH3 HO CH2 CH2…
A: The objective of the question is to find the meso compound from the given options which is also an…
Q: 1. The lab manual suggests an alternate strategy for the separation of aspirin from caffeine - that…
A: The discussion of the preceding questions centres on organic chemistry laboratory processes,…
Q: ■ct: Br Click and drag to start drawing a structure. NaOH Ö Click and drag to start drawing a…
A: Product of following reaction can be made by applying appropriate reaction mechanism.
Q: Find/show all possible symmetry operations and the point group of the following compounds by drawing…
A: The objective of the question is to show all possible symmetry operations and the point groups of…
Q: synthesis from butane to 3-methylheptane
A: The synthesis of 3-methylheptane from butane involves several steps, including chain elongation and…
Q: A 30.0 mL volume of 0.169 M HCO2H (formic acid, Ka = 1.8x10-4) is titrated with 0.474 M NaOH.…
A: Here, Given information are,Volume of Formic acid= 30.0 mlKa value of Formic acid= 1.8×…
Q: A weak acid, HA, is a monoprotic acid. A solution that is 0.220 Min HA has a pH of 2.440 at 25°C.…
A: The objective of this question is to calculate the acid-ionization constant, Ka, for the weak acid…
Q: + CH3Mgl H 1. Dry Et₂O 2. aqueous HCI at 0°
A: This reaction is the formation of alcohol from aldehyde using a Grignard reagent. Grignard reagent…
Q: Please don't provide handwriting solutions....
A: The objective of the question is to identify the elements among Be, C, Fe, Ca, Ne, Zr that have no…
Q: 2. Give the IUPAC name F H&C. CI L CH3 H₂C
A:
Q: O eq. NaOH oby excess H₂O H2SO4 catalytic
A: Acidic hydrolysis of ester give carboxylic acid and alcoholBasic hydrolysis of ester give sodium…
Q: Which Newman projection represents correct conformation for the following compound: A HO C H3C. CH3…
A: The two-dimensional representation of a 3D molecule along the C-C bond is known as the Newman…
Q: 2. Mechanisms and molecular structure: a) The following reaction can happen in cells with the help…
A: The objective of the question is to understand the molecular structure and mechanisms of a reaction…
Q: :Br " Complete the mechanism for the following reaction. Draw all indicate movement of electrons,…
A: Formation of cyclic boromonium ionIntramolecular nucleophilic substitution
Q: Consider the following reaction: H2(g) +Se(g) H2Se(g) The data in the table show the equilibrium…
A: Temperature (K)1/TEquilibrium Constantln Keq10000.001004.9 x 10513.1010250.000972.8 x…
Q: Which of the following statement is NOT CORRECT about bond polarity? O a. All carbon-based compounds…
A: A polar covalent bond exists when atoms with different electronegativities share electrons in a…
Q: In the boxes provided below, draw a mechanism to show the formation of the cyanohydrin. Include all…
A: Final answer is given in explanation please see from there.Explanation:Approach to solving the…
Q: Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side…
A: Carbonyl compounds (aldehyde and ketone) react with an alcohol to form hemiacetal in the presence of…
Q: Draw the final product of the reaction sequence catalyzed by glycolysis. Provide the structure in…
A: Given question based on glycolysis. The given starting compound is glucose.
Q: Each of the following molecules has one stereocenter. Identify the stereocenter in each and draw…
A: Answers are discussed in the explaination box.Explanation:Approach to solving the question:Stereo…
Q: Pure phosgene gas (COC12), 0.0300 mol, was placed in a 1.60 L container. It was heated to 850.00 K,…
A:
Q: Consider the equilibrium system described by the chemical reaction below. For this reaction, Kc =…
A: The objective of the question is to determine the equilibrium concentration of HF in a chemical…
Q: Theoretical and practical chemistry are sometimes two different things. In theory the reduction of…
A: Given:Reaction: reduction of benzil to hydrobenzoin using NaBH4 and H2O could be done with lithium…
Q: Can you give a balanced chemical reaction for nitration of benzonitrile to 3-nitro benzonitrile?
A: The answer to the question is given below.Explanation:Step 1:The nitration of benzonitrile to…
Q: What is the major product? 1) Ph-CH,-M¤Br 2H i OH Ph OH I Ph Ph Ph
A: The reactant is an aldehyde. It is an organic compound. The reagent is a Grignard's reagent that…
Q: Only typed solution
A: The objective of this question is to calculate the pH at the equivalence point of a titration…
Q: Identify how many N (NITROGEN) atoms have sp³ hybridization for the compound below:
A: Hybridization is a process by which the atomic orbitals of an atom interact with each other to form…
Q: The ionic radii of element E and a different metallic element, M, are shown in the following table:…
A: The objective of the question is to determine whether the lattice energy of MO would be less than,…
Q: Please do 27, draw and explain the reagents options if possible
A: Correct answer is (a)Explanation:Step 1: Step 2:Step 3: Step 4:
Q: Only typed solution
A: The objective of the question is to determine the pseudo-first-order and second-order rate constants…
Q: Propose a chemical structure for the name below. Make sure to clearly define the stereochemistry…
A: IUPAC Rules for the nomenclature of the branched organic compoundsFirst we should select the longest…
Unlock instant AI solutions
Tap the button
to generate a solution
Click the button to generate
a solution
- 1. Show a detailed mechanism for the following reaction. 1. Cl2, NaOH HO. 2. H3O* 1Complete the mechanism for the reaction between acetone in acid and bromine by adding the missing bonds, atoms, charges, nonbonding electrons, and curved arrows (forward reaction only). Step 1 "-" H 10: Ć H Step 3: bromine is added. Complete the structure and add curved arrows. Select Draw Templates More H 0 Br *** HO-H 1 H Q2Q Step 5: alter the water or bromide to give the final products. Select Draw Templates More ||||||||||| H Br Erase HO: H Erase pa Step 2: complete the structure and add curved arrows. Select Draw Templates More |||||||||| H 3 Select Draw Templates More 0 Step 4: complete the structure and add curved arrows. 3 Ć Q2Q ||||||||||| H 0 Br H Erase ** Erase aaª]3. Provide the mechanism for the following reversible nucleophilic addition. Show all curved arrows and intermediates. cat. H+ H₂O HO OH H H 1) protonate to activate 2) nucl adds 3) deprotonate what stays
- Step 1. Protonation of carboxylic acid. Draw curved arrows. Select Draw Rings More Erase | 7|/ C H |- H HöH H H : 0 : H H Step 2. Nucleophilic attack by alcohol. Draw curved arrows. Select Draw Rings More Erase H Step 3. Proton Transfer H. CH :0Complete the mechanism and draw the final product for the Grignard reaction. Step 1: Add curved arrows. Select Draw Rings More Mg Erase Br Et₂ O Step 2: Aqueous workup. Complete the intermediate, then add curved arrows for the workup step. Select Draw Rings More -Ï- H H Mg EraseDraw the product(s) of the reaction below. CEN: Add/R.
- Number 8 please. Is this answer correct? And can you please show the mechanism?Complete the mechanism below by adding curved arrows on the reactant side and drawing the products. Be sure to include lone pairs and charges if applicable. 可 H₂C CH CH ci HO: H H CH2CH3 + Add/Remove step 2 Click and drag to start drawing a structure.Step 2 Correct. In step 2 (loss of a leaving group, by collapse of a charged tetrahedral intermediate), a carbonyl group is reformed and the excellent chloride leaving group is ejected, as shown with two curved arrows. Add two curved arrow(s) to show step 2: collapse of a charged tetrahedral intermediate. Modify the given drawing of the product as needed to show the intermediate that is formed in this step. Use the +/-tools to add/remove charges, and use the single bond tool to interconvert between double and single bonds.
- 6. Multi Step Synthesis. Propose a synthetic route from the reactant to the product using any reagents you need. Nalt LINH4Be sure to answer all parts. 9. Draw one resonance structure for each of the conjugate bases formed by removal of the labeled protons (H2, Hp, and H) in cyclohexane-1,3-dione. Rank these protons in order of increasing acidity and explain the order you chose. 10 points Ha H. еВook Print cyclohexane-1,3-dione References Part 1 out of 3 Draw one resonance structure for each of the conjugate bases formed by removal of the labeled protons (H2, Hp, and H) in cyclohexane-1,3-dione. Don't forget to include lone pairs in each structure. draw structure ... draw structure ... draw structure .. Ha removed Нь removed H. removedThis question has multiple parts. Work all the parts to get the most points. a The following compound was synthesized from the reaction of an acetylide ion with a carbonyl compound (i.e. an aldehyde or a ketone), followed by a reduction. OH CH3CH2CH2CCH=CH2 ČH»CH2CH3 Draw the structure of both the aldehyde/ketone and the acetylide ion that were used. • You do not have to consider stereochemistry. • Do not include cationic counter-ions, e.g., Na", in your answer. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate structures with + signs from the drop-down menu. Previous