Retrosynthetic Analysis Question In the box draw the two possible starting materials you could use to synthesize the following molecules using the reaction indicated. Nucleophilic Subsitution Reaction Nucleophilic Subsitution Reaction Nucleophilic Subsitution Reaction Nucleophilic Subsitution Reaction followed Acid Catalyzed Hydration of Alkyne Nucleophilic Subsitution Reaction followed by hydroboration Oxidation of Alkyne H
Q: Please Write Step by Step Solution Otherwise I give DISLIKE !!
A: Thank you.
Q: Sagar
A:
Q: please answer in text form and in proper format answer with must explanation , calculation for each…
A: In case of any doubt please feel free to ask.
Q: None
A: The IUPAC nomenclature of organic compounds follows this naming format:Writing the name of organic…
Q: If you are interested in separating a mixture of volatile compounds, which technique do you think…
A: The objective of the question is to identify the best technique for separating a mixture of volatile…
Q: i dont want hand writting image
A: You asked for no handwritten structures i hope these are understandable.
Q: [M(OH2)6]2+ is a vivid green color in aqueous solution. The complex [ML6]2+, where L is a…
A: To analyze this problem, consider the concept of crystal field theory, which describes how ligands…
Q: At a particular temperature, the solubility of In2(SO4)3 in water is 0.0061 M. What is the value of…
A:
Q: For the aqueous [Hg14] complex K, -6.76 × 1029 at 25 °C. 2+ Suppose equal volumes of 0.0092 M Hg…
A:
Q: work 12:Acetal Chemistry work Due in a day Homework ○ 7/13 answered Draw the product of the…
A:
Q: please give Step by Step Solution otherwise i give you DISLIKE !
A: Step 1: Abstraction of proton. Step 2: Formation of enolate. Step 3: Alkylation. Step 4:
Q: Predict the major product of the following reaction below. ام HNO3 H₂SO4
A: Step 1: Step 2:Mechanism Step 3: Step 4:
Q: why electron affinities for halogens are all negative but the electron affinities for the noble…
A: Step 1:The electron affinity measures the energy change when an atom gains an electron. For…
Q: Please don't provide handwritten solution .....
A: Step 1:Aldol reaction:-Aldol reaction combines two carbonyl compounds by making a C-C bond. This…
Q: What is the systematic name for this compound? O 3,decyne O 3-nonyne O 3-decyne O 3-hexyne O…
A: So, the answer is 3-decyne.
Q: None
A: Step 1:Stability of conjugate acid is less => More basicElectronegative: C < N < O Step…
Q: Predict the major product formed when the compounds shown below react with each other under the…
A: Step 1:Given reaction in known as Diels-Alder reaction.The Diels-Alder reaction involves a diene and…
Q: What would be the major product(s) of the following reaction? །། Brtw HO 20°C (CH3)2CHCH20 I…
A: Tertiary alkyl halide in the presence of alcohol will either undergo SN1 (nucleophilic substitution…
Q: Draw and explain the diagram of molecular orbitals of 1,3,5,8-octatetraene, label the followinga)…
A: ### **Step 1: Count π Electrons**1,3,5,8-octatetraene has eight π electrons, contributed by each of…
Q: IV = II Use the letter (a-k) in the box provided for the reagent required for the each of the given…
A:
Q: www-awu.aleks.com/alekscgi/x/Isl.exe/10_u-IgNslkr7j8P3JH-IQUHIQg6bJxmeSyVPHOEB1plef9xyC5Ca9Qllg7siQ-…
A: Step 1:naming process for each molecule:1. 2-Hydroxybutanal a. Identify the Longest Carbon Chain…
Q: Provide a procedure for the synthesis of "L-gulono-Lactone" from "D-gluconic acid lactone"
A: The objective of the question is to provide a procedure for the synthesis of "L-gulono-Lactone" from…
Q: Increasing Energy 15. Complete the electron configuration diagram below for a neutral Sb atom. 7p 6d…
A:
Q: = O Kinetics and Equilibrium 2/5 Bi Calculating an equilibrium constant from a heterogeneous…
A: Given: V=8.3Lmass,gMolarmass,g/mol2Hg(l)7.2200.59+O2(g)15.432.00→2HgO(s)11.7216.59Step 1:…
Q: Probide a synthetic pathway D O OH HH X
A:
Q: A ALEKS - Julianna Graham - Lex ← ->…
A: Step 1: Rules of IUPAC nomenclature can be given asIdentify the Longest Carbon Chain as this chain…
Q: Provide the mechanism for the following reaction (1) PhMgBr (2 equiv) (2) H3O+ workup OH
A: It's not a methyl group in the product, it should be a phenyl group because there is no source of…
Q: 8. Give the final product 1) [H+], E+ OH (2 eq) 2) Me Mg Br 3JH20 4)430+ OH a) رها он он Ј I
A: In case of any doubt feel free to ask.
Q: None
A:
Q: None
A: The reaction is to be balanced in the basic medium, so we will use the charge balance method:First…
Q: what is period 2 group 7 element symbol
A: Step 1:
Q: A galvanic (voltaic) cell consists of an inert platinum electrode in a solution containing 1.0 M…
A: Temperature is 25oC or 25 + 273 K = 298 K. Given that concentration of each ion is 1M. Standard…
Q: None
A: This reaction represents the conversion of a carboxylic acid derivative (CI-ONa) to a carboxylic…
Q: Propose a reasonable, detailed stepwise mechanism, using curved arrow notation to show the flow of…
A: Approach to solving the question: Detailed explanation: Examples: Key references:
Q: From Halogen form a structure of a haloalkane (alkyl halides)
A: Step 1:
Q: 0.10 M potassium chromate is slowly added to a solution containing 0. 50 M AgNO3 and 0. 50 M…
A: Given:K2CrO4=0.1 M Ksp Ag2CrO4= 1.1 × 10-12AgNO3= 0.5 M Ksp BaCrO4= 1.2 ×…
Q: dont provide handwriting solution....
A: A spanning tree of a connected graph is a subset that includes all the vertices of the original…
Q: a.)Identify structure of the compound and draw the moleculeb.)Analyse HNMR peaks for (A AND B)C.…
A: HNMR Spectra AnalysisThere are only two types of protons so only two singlet are obtained as we…
Q: None
A: This is reduction of amide into amine with lithium aluminum hydride, a very strong reducing…
Q: What volume of 5.00 × 10-3 M HNO3 is needed to titrate 80.00 mL of 5.00 × 10-3 M Ca(OH)2 to the…
A: Reaction involved is 2HNO3 + Ca(OH)2 -> Ca(NO3)2 + 2H2OAccording to reaction 1 mole of Ca(OH)2…
Q: Bioremediation is a promising technology for effective, inexpensive treatment for trichloroethene…
A: In aerobic conditions, the reaction occurs in the presence of oxygen, and in anaerobic conditions,…
Q: Sally is planning for Part C of the Trends in the Periodic Table lab. Which chemicals would be…
A: The objective of the question is to identify the appropriate chemicals that Sally can use to…
Q: None
A: Among the carbonyl compounds the acidity is determined by the reactivity of the carbonyl compounds.…
Q: period 2, group 7 element symbol
A: Step 1:
Q: For this question: How SPF blocks UV Rays from the sun Please try to answer it in a presentation…
A: Ultraviolet (UV) radiation is a type of electromagnetic radiation that is produced by the sun.…
Q: 8.) Consider the following equilibrated system: 2NO2(g)=2NO(g) + O2(g). If the Kc value is 0.918,…
A:
Q: Step 3 Add two curved arrow(s) to draw step 3 of the mechanism: collapse of a charged tetrahedral…
A: Step 1: Step 2: Step 3: Step 4:
Q: Please provide explanations regarding IUPAC rules
A:
Q: Show mechanism and product for each of the following. In any aldol reactions, be sure to show any…
A: Step 1: Aldol condensation reaction is the reaction between two molecules of aldehydes reacted in…
Q: :$;$;$;$$:$$:$;$
A: Step 1: Step 2: Step 3: Step 4:
Step by step
Solved in 2 steps with 4 images
- This is Wittig Rxn: Whatever mechanism you choose to draw is fine since you can leave the base as B: Draw the arrow pushing mechanism using the compounds below – Constant: 4-nitrobenzyl benzaldehydebase 1: triethylaminebase 2: NaOHbase 3: K2CO3ylide: Acetonyltriphenylphosphonium chloridePropose how you could synthesize the following compound, using a substitution reaction. Propose a nucleophile, a solvent, and an electrophile. Show the curved-arrow mechanism of the reaction. Finally, draw the transition state of the reaction.Indicate which of the ff. statements regarding nucleophilicity is incorrect. 1. F- is more nucleophilic, hence, more reactive towards methyl iodide than Cl-. 2. Second-row elements are more nucleophilic than first-row elements of comparable basicity. 3. Nucleophilicity is the affinity of a nucleophile to an electrophilic carbon. 4. The rate of SN2 reaction may be markedly affected by the nucleophilicity of the attacking atom
- Rank the nucleophiles in following group in order of increasing nucleophilicity. −OH, Br−, F− (polar aprotic solvent)Using the diagram below, answer the ff. questions.1. What pattern of curved arrow pushing is the second step of this reaction?a. loss of a leaving groupb. proton transferc. rearrangement 2. What pattern of curved arrow pushing is the fourth step of this reaction?a. proton transferb. loss of a leaving groupc. nucleophilic attackConsider the mechanism of a reaction below Aniline (with NH2) above acts as ____________________ Lewis base and a nucleophile Lewis acid and a nucleophile Lewis base and an electrophile Lewis acid and an electrophile none of the above Draw a RESONANCE STRUCTURE (major contributor please) of the product. Please use curved arrows to push electrons:
- Draw the structure(s) of the major product(s) of the following reaction after workup to neutralize acid. You do not have to consider stereochemistry. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Include the counterion when the product is a quaternary ammonium salt. Draw the counterion in its own sketcher. Separate multiple products using the + sign from the drop-down menu. If no reaction occurs, draw all starting materials.Synthesis: A Hormone Herbicide please draw the molecules and explain 1. Draw benzene + methanol + acid catalysis = Hormone Herbicide intermediate 1. 2. Draw Hormone Herbicide intermediate 1 + fuming sulfuric acid + heat + time = Hormone Herbicide intermediate 2. 3. Draw Hormone Herbicide intermediate 2 + HNO3/H2SO4 + heat = Hormone Herbicide intermediate 3. 4. Draw Hormone Herbicide intermediate 3 + water + heat = Hormone Herbicide intermediate 4.5. Draw Hormone Herbicide intermediate 4 + H2/Pd = Hormone Herbicide intermediate 5.6. Draw Hormone Herbicide intermediate 5 + NaNO2/HCl = Hormone Herbicide intermediate 6.7. Draw Hormone Herbicide intermediate 6 + CuOH = Hormone Herbicide intermediate 7. 8. Draw Hormone Herbicide intermediate 7 + Cl2/FeCl3 = Hormone Herbicide intermediate 8.9. Draw Hormone Herbicide intermediate 8 + NaOH = Hormone Herbicide intermediate 9.10. Draw Hormone Herbicide intermediate 9 + 2-chloroethanoic acid = A Hormone Herbicide.Synthesis: A Hormone Herbicide. Please draw the molecules and explain 1. Draw benzene + methanol + acid catalysis = Hormone Herbicide intermediate 1. 2. Draw Hormone Herbicide intermediate 1 + fuming sulfuric acid + heat + time = Hormone Herbicide intermediate 2. 3. Draw Hormone Herbicide intermediate 2 + HNO3/H2SO4 + heat = Hormone Herbicide intermediate 3. 4. Draw Hormone Herbicide intermediate 3 + water + heat = Hormone Herbicide intermediate 4.5. Draw Hormone Herbicide intermediate 4 + H2/Pd = Hormone Herbicide intermediate 5.6. Draw Hormone Herbicide intermediate 5 + NaNO2/HCl = Hormone Herbicide intermediate 6.7. Draw Hormone Herbicide intermediate 6 + CuOH = Hormone Herbicide intermediate 7. 8. Draw Hormone Herbicide intermediate 7 + Cl2/FeCl3 = Hormone Herbicide intermediate 8.9. Draw Hormone Herbicide intermediate 8 + NaOH = Hormone Herbicide intermediate 9.10. Draw Hormone Herbicide intermediate 9 + 2-chloroethanoic acid = A Hormone Herbicide EXPLAIN PLEASE!
- select the most appropriate reagent(s) to effect the change. K2Cr2O7, H+ H2, Pd 1. Disiamylborane, 2. HO–, H2O, H2O2 NaOCl H2SO4, HgSO444. Sterically hindered bases produce what is the major product? Zaitsev product Hoffman product Markovnikov product Anti-Markovnikov productA4 Express the retro synthesis scheme using the suggested starting material (SM) for the following target compound (TM). After performing the retro synthesis analysis, synthesize the target compound according to the analyzed scheme.