Q: N MgBr 1. 2. H3O+
A: This is addition of Grignard reagents to nitriles to give ketones after hydrolysis.
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A: The possible two synthetic routes are given below -
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A: Time (s)Concentration of A (M)00.640 1860.4153720.190
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Q: Calculate the pH of 0.075 M NaOH. O 13.26 O 12.88 O 11.12 O 11.46 10.40
A: NaOH is a strong base thus dissociates completely in solution asNaOH -------> Na+ + OH-Therefore[…
Q: How many grams per four moles are there in Nitrogen? O 1.008 24.022 48 56.028 5.04
A: The objective of the question is to find out the mass in grams of four moles of Nitrogen.
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A: Given,The compound: CyF3CyF3 dissociates into Cy3+ and F- ions.Ksp ( CyF3 ) = 6.97 x 10-4
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A: The objective of the question is to find which of the given following statement is generally true.
Q: Write a name for the following organic compound- H₂C CH₂ CH₂ H3C-C-CH₂ CH₂ H₂C CH3 1² CH₂-CH3
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Q: Br Mg+ Br + ether -780 ? a. b. C. Br d. Br Mg
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Q: analyse this ir spectrum
A: The detailed ans has been attached. Explanation:3033 cm^-1: Likely due to sp^2 C-H stretching…
Q: What are the steps and reagents needed to synthesize this molecule?
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Q: etermine the average rate of change of B from 1=0s to =372 s. A 2B Tim 3
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Q: m. LOCH 3 12 H2O2 H2SO4 n. CN O. p. NH2 HNO3/C H2SO4 NBS H2O2 Br NBS 。 H₂O2 A
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Q: 2.Label the following as R or S a. b. NH2 H Br T H d. HO HO H₂N H
A: The objective of the question is to predict R and S configuration for the following given molecules.
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what are the steps and reagents needed to synthesize this molecule?
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- Use the following molecules to sneer the worksheetring Part A H2C=CH-CH2 CH2-CH3 Spell out the IUPAC name of the compound. ols hex-2-ene Submit Previous Answers Request Answer X Incorrect; Try Again; 7 attempts remaining Part B Br Spell out the IUPAC name of the compound. 3-bromo-1-butyne Submit Previous Answers Request AnswerYou may want to reference (Pages 408 - 414) Section 12.3 while completing this problem. The compound frambinone has the taste of raspberries and has been used in weight loss. Its structure is HO |||-CH₂-CH, -C-CH3 ▾ Part A Identify the functional groups in frambinone. Check all that apply. ketone aromatic aldehyde ester ether phenol Submit Request Answer
- IZ4n9Qu4wHIZKigV5NXnNV9pn4HUbA/formResponse Your answer Write the IUPAC name of the molecule shown below. Your answer Po WAnswer the following questions1. Give the IUPAC name of the compound in the first picture below2. Why is the reaction between these compounds not favorable (second picture ) ? State the rkind of eaction and describe why it's not favorable.Predict the product of the following reaction. Excess Raney Ni, H2 Name the product using the IUPAC naming rules. Determine the molecular formula of the product. List atoms in alphabetical order.
- Please give me answer fo this IUPAC namesAnswer the question below. Please go through each step in great detail.Please answer this Can you give examples to explain Addition reactions-general characteristics Benzene rings do not reactthi like alkenes Remember, the electrophile adds to the less substituted carbon, and the nucleophile to the more substituted carbon. Markovnikov’s Rule: The addition of a hydrogen halide to an alkene favors the product in which the proton adds to the alkene carbon that is initially bonded to the greater number of hydrogen atoms. Carbocation rearrangements- Methyl groups and hydride groups can migrate to make a more stable carbocation. A primary carbocation is less stable than a secondary carbocation, which is less stable than a tertiary carbocation. Addition of A Strong Bronsted Acid Hydrohalogenation HX addition to an alkene. Goes through a carbocation intermediate. The electrophile (H+) adds to the less substituted carbon, and the carbocation forms on the more substituted carbon. The nucleophile (X-) then adds to the more substituted carbocation.…