Q: [OH-]
A:
Q: e basic anions?
A: This is a multiple questions. According to guidelines in multiple questions, we can solve only the…
Q: Et H Me Me Me Me H. Et Me H. Me iPr, H H H. -Me Me D. Me H H iPr `Me
A:
Q: cat. H-A MeO HO MeOH +
A: Through Reaction mechanism we can find the slowest step of the reaction which is also known as Rate…
Q: CH, H,C CI
A:
Q: 1. NaOH 2. CH3CH,CH,Br 3. НСI, Н2О 4. NaOH N-H CH3CH2OH, HCI OCH3
A: Introduction : As per company norms we cannot answer more than three subparts .So, I have answered…
Q: H H C.
A: Polymers are very large molecules which are formed by monomers. When monomers repeats continuously…
Q: Please answer the pOH, [H3O+], [OH-]
A: Given,
Q: (a) CEN-Ph CH2 NPh
A: Since you have posted multiple independent questions in the same request, we will solve the first…
Q: con jugate base. CH3alt Cat-Tsolf
A:
Q: B) O2N- CO D) H3C- -COOH
A: As we know, Carboxylic acid (-COOH) is more acidic than Alcohol (-OH). Now, In organic compound, if…
Q: 요 он + + H₂N -N- H O_H "NH₂ HCI e troce acid >
A:
Q: Predict the major c Select Draw 1. NaOEt/E1OH 2. E1OCOCH,Br 3. dilute NaOH, heat 4. H30* 5. Heat но
A: Active methylene compounds are very acidic proton. Active methylene compounds have two acidic…
Q: КОН CH;COOH HO -H- ОН 1) Ph2Cul H3O* 2) H3O* Li N. 2) H,0*
A: The question is based on the concept of organic reactions. we have to identify the Product formed…
Q: A ) mePBA 2) Hcl/ THF Ch ater) B He and pd/C -> EtoH )ko BUABUOH 2) Btz then Fa 2/ NaoH/ HaO Br
A: A. Epoxidation olefin followed by epoxide opening with chloride ion. B. Hydrogenation of alkenes. C.…
Q: the pic (yellow circle l). What is the above O means? Is it 5OH^- or 5 O^- H?
A: Oxidation means loss of electrons and reduction means gain of electrons.
Q: OH H- OMe TSOH, H20 OMe
A:
Q: -OH- CI
A: Protonation of O-atom of epoxide . Attack to nucleophile to the most substituted side.
Q: H;PO4 OH
A: First H+will add on anion and carbocation willl form and oH will add on carbocation after reaarange…
Q: NH2 Me b) Me Me NH2 H,SO, (cat.) Me
A:
Q: NH2 NH2
A:
Q: NH2 Et3N
A:
Q: 1.1 equivalent LDA, -78 °C 2. CH;CH,Br
A: LDA preferentially abstracts proton form less - sterically hindered site because it is a bulky base.…
Q: HN-CO Но- но, HO ÇI HO Но- Но- `NHẠC H H „NH2 N. H H H HN HOOC HO Он но OH -OH OH OH Teicoplanin
A: Given, Teicoplanin
Q: May you please help me with this ochem question?
A: Option-3 is the correct answer
Q: H* `NH2 OH o NaBH4 OEt ELOH OEt но 04 OH OH H30* H20
A: Given reactions,
Q: HO- 1. Hg(OAc)2, 2. NaBH4 NaOH Br HO,
A:
Q: CH;NH2
A: Primary amine react with unsaturated ketone to form beta - amino ketone.
Q: *Lo00 wt-2, NaoH : 0.1N
A: Normality : It is number of gram mole of solutes present or dissolved in 1 litre of solution.
Q: NaOH on? 0° C
A: The question is based on the concept of organic reactions. We have to identify the product formed in…
Q: CHO H- HO- NaBH4 H- H OH HO- Но- ??? CH2OH A. В. С. CH2OH СООН COOH H- HO- HO- HO H HO H HO H. HO- -…
A:
Q: cat. H-A MeO MeOH
A: Protonation of esteral oxygen Attack of alcohol as nucleophile (intramolecular) Loss of leaving…
Q: HCI/Ethe H,C
A:
Q: 15. The correct IUPAC name for the compound for med by the reaction be low is OH + HSQ, HC OH
A:
Q: а) ? H OH OH b) ?
A: The given reaction can be completed as follows:
Q: Draw curved arrows to show where the electrons start and where they end in the following reactions:
A: A chemical reaction is symbolic representation of the conversion of substances to new substances. In…
Q: А. B. С. D. ночо HO H НО HOH H IIOI нно H H H H-OH H -OH CH₂OH CHO -OH H- -OH HO OH CH₂OH H HO -H H…
A:
Q: HạC NH,
A:
Q: HN- H,OH+
A:
Q: H,O 4 NaOH/H,O 12/KI (exceso) a. AGNO3 NH OH Br2 (1 mol) b. HOẠC etanol KOH/EŁOH с. KOH/ELOH
A:
Q: 3-28 Dreaw the méch CN NAOH ce OH ph
A: a) 3-chlorobenzonitrile reacts in the presence of base as sodium hydroxide and water under heating…
Q: 1. OH H2SO4 HO. 2. NABH4, ELOH
A: First Ketone group will protonated by the gain of H+ then nucleophile OH attack on carbonyl carbon…
Q: S. Which compound is Anheni acid? A HS0, R KCI C NOH D NH,
A: 5. Given compounds, A. H2SO4 B. KCl C. NaOH D. NH3
Q: acid FÓRMULA pKe1 pK.2 pK23 pK«4 Он HO-C-CH2-C–CH2–Ĉ–OH 2.94 4.14 5.82 16.0 0=C-OH
A: HA <===> H+ + A-
Q: Nao H- Keq =
A: I am explained you this reaction not going to forward direction means right side. You can see the…
Q: 1) LAH 2) H30* HO. none of these HO OH он ...
A: In this question given the reaction with lithium aluminum hydride, with cyclic easter, another…
Q: th cl Nliph Alke Aro
A: Hydrocarbons can be defined as the organic compounds containing hydrogen and carbon atoms.
Q: 3) NH4 (aq) + NH3 (aq) + H30" (aq)
A: The question is based on the concept of equilibrium. we are titrating a strong acid with a weak…
Q: H CH — С — Сн, OH
A:
Just want to check whether its right
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- 2. How many substitution product/s is/are formed when metabromo anisole is treated with ammonia?A. 0-no reactionB. 1C. 2D. 3Melamine, used as a fire retardant and a component of the writing surface of white boards, can be prepared from s-trichlorotriazine through a series of SNAr reactions with ammonia. The first substitution takes place rapidly at room temperature. The second substitution takes place near 100 °C, and the third substitution requires even higher temperature and pressure. Provide an explanation fatr this reactivity.When 3-methyl-1-butene is reacted with 9-borabicyclo[3.3.1]nonane, the "1-ol" product is formed. What is the detailed reactin scheme for the transformation? Describe the purification procedure.
- 2) What is the main product for each of the following reactions? (d) Styrene + CH3CH2COCl AlCl3, then Br2, Fe -----> ? (e) Benzene + 1-chloro-2,2-dimethylpropane, AlCl3 -----> ? (h) Benzene + HCOCl, AlCl3 then 1-chlorobutane, AlCl3 -----> ?N(CH2CH3)3 + HNO3 --------> a.) rewrite the reaction using bond-line structure of reagents and products of the reaction b.) supply the curved arrows explaining the mechanism of the reactionComplete the flowchart by drawing the resulting structures of each reaction. A. B. C. D. E. F. G. H. I.
- a.What product(s) (excluding stereoisomers) are formed when Y is heated with Cl2? b.What product(s) (excluding stereoisomers) are formed when Y is heated with Br2? c.What steps are needed to convert Y to the alkene Z?What steps are needed to prepare phenylacetylene, C6H5C = CH, from each compound: (a) C6H5CH2CHBr2; (b) C6H5CHBrCH3; (c) C6H5CH2CH2OH?Alkyl halides undergo elimination reactions with Brønsted–Lowrybases. The elements of HX are lost and an alkene is formed. Explain this ?
- Chemistry 60. Give the principal product(s) expected, if any, when trans-1,3-pentadiene reacts under the following conditions. Assume one equivalent of each reagent reacts unless noted otherwise. (a) H2O, H3O+ (b) Na+EtO- in EtOH (c) Maleic anhydride heatWhat is the major product fromed from the reaction below?Provide a reasonable arrow-pushing mechanism for Reaction 5b, and explain the the stereochemical outcome. 5d below