Q: please give correct product with mechanism ( confuse it is Sn1 or Sn2 ) answer only if u are sure ,…
A: The following concept is used to solve the above question with the perfect àpproach . Polarity…
Q: Please rectant and product name and give ?mark
A: Solution- Reactant and product and reagent name are given below by the above reaction-
Q: Please help me solve this synthesis. It takes 5 steps
A: OKAY, I will give complete synthesis by using 5 steps. You can see step by step solution. How to…
Q: Br NaOEt ELOH
A:
Q: Please draw chemsketch of this by using any software like kingdraw or chem draw. And send this…
A:
Q: How
A: We will write the mechanism
Q: кон "Br
A: In anti elimination, the base attacks the β-hydrogen on the opposite side of the leaving group. It…
Q: H. NH2
A: The reaction taking place is given as,
Q: For next 2 problems, include a TS arrangement of hydroboration step that explains regioselectivity.…
A: When an unsymmetrical reagent is added to an unsymmetrical alkene then the negative part of the…
Q: 1 Optically active 2 Capable of forming a zv neutral solution id
A: 2-aminopranoic acid is given and three statements are given and asked which is/are true.
Q: In Part 1, draw a mechanism for the reaction of ammonia with butanoic acid. In the box to the left,…
A: Butanoic acid (CH3CH2CH2COOH) is a weak acid, and ammonia (NH3) is a weak base. Hence they will…
Q: This will require more than one step of reagents to arrive at the final product. Write the…
A:
Q: OTs NaOEt ELOH
A:
Q: What are the major products of these reactions (pls show the mechanism so i can understand how to do…
A: Hello. Since the question contains multiple subparts the first three subparts are solved. In case…
Q: unfortunately, I am asking for the name of the product
A:
Q: What are the major product(s)? Show all the arrow push mechanism.
A: Biomolecular elimination (E2) reaction: E2 reaction involves a one-step mechanism in which…
Q: whats the product name from reaction below?
A: This is a question from organic reaction.
Q: Hello,can you help me with these please.
A: Since you have posted a question with multiple sub-parts, we will solve first few sub-parts for you.…
Q: drawing the major product(s) of hexane, iodine and light
A: Alkanes undergo reaction with iodine molecule (I2) to form the halogenated product. This reaction…
Q: What is the major product(s)? Show the arrow push mechanism.
A: It is an example of E2 elimination reaction
Q: Show the first step in the hydroboration mechanism using the reagents below.
A: In hydroboration - oxidation of alkene , there occur addition of H2O (anti-markonikov's addition) In…
Q: NaOH Br NaOH NaOH Br NaOH NaOH Br
A: In elimination reaction, substituents present in the reactant are eliminated giving rise to product.…
Q: What is the name of the final products that are shown here?
A:
Q: Predict the product of the reaction below. NaOH and heat
A:
Q: Could
A: Since you have asked a question with multiple sub-parts, we will solve first three sub-parts for…
Q: 2. Predict the product and show mechanism.
A: When a carbonyl compound reacts with a primary amine, we get an imine.
Q: Work backwards from the product by asking: What type of reactionsintroduce the functional groups in…
A: The functional group are the groups attached to the chemical compounds which change the properties…
Q: NaOH OCH3 OCH3
A:
Q: The
A: Ketone react with ethanol then we get acetal product. First ketone protonated by the gain of H+ then…
Q: Please draw the product(s) and please answer questions A through E
A:
Q: Predict the products and please show all arrow pushing
A: LiAlH4 is reducing agent and prefer 1,2 addition in case of alpha- beta unsaturated carbonyl…
Q: Can you explain the mechanism? Can you provide a shortcut?
A:
Q: HONH, CI- , NaOH
A: This is an example of condensation reaction in which hydroxylamine condensed with 1,3-dikketone to…
Q: Na NH3() diene
A: Reaction of alkynes with Na/NH3 produces alkene. This reaction is stereospecific and gives only the…
Q: Please help with showing the step and explaining the result with answer, thank you
A: The reaction that will take place is Cu2O + H2 -----> 2 Cu + H2O
Q: 2. HCI Caz) uorkup
A: Acid chloride reacts with the two moles of the Grignard reagent to form tertiary alcohol. The…
Q: Synthesis. Complete 2 of the 3 syntheses below. Show a reaction, or series of reactions, you could…
A: 1. Friedel craft's alkylation : benzene reacts alkyl halide in presence of lewis acid like AlCl3…
Q: The second page is an example how it suppose to be done. (Hex-4-en-3-one+CH3CH2MgBR). It's…
A: The equation would normally be written: You can think of primary amines as just being modified…
Q: Can you please help show how to appraoch this problem and eleaborate the steps.
A:
Q: How do you confirm reaction and product. Please show curved arrows and provide written explanation…
A: A chemical reaction is a cycle that prompts the compound change of one group of compound substances…
Q: to show all possible products and if appropriate,
A: a) Hydrocarbons like alkane, alkene and alkynes undergo combustion reactions with oxygen (O2) and…
Q: OH3C HCO- 1 hoi H 2 1) C4HgLi 2) THF OH3C ΗΤΗ H OIS H 3
A:
Q: Br O 'H H 2. H₂0 Mg/ether 1
A: Alkyl/aryl halides are converted into alkyl/aryl magnesium halides upon treatment with Mg(0) in…
Q: Choose one example from the set of synthesis reactions in Model 1
A: In model-1 there is a different types of chemical reactions are given 1. Combination reactions ( set…
Q: Use retro synthesis analysis to break down the molecule into at least 4- 5 starting compounds. HO I…
A: Retro synthesis is the conversion of the target compound to its precursor or simpler structures.
Q: Please complete the reactions given below.
A: Given reactions: g) h) i)…
Q: Just write products dont need detailed reactions thanks
A: Hello. Since the question contains multiple sub-parts, the first three sub-parts shall be solved…
Step by step
Solved in 2 steps with 1 images
- -PProvide reagents capable of accomplishing the transformations below. Some may require more th alSne step. You may use any reagent from the reagent page, or any combination of those reagents, or any other reagent that contributes fewer than 5 carbons to the final product. 6. но. b) OCH3 LOCH, c) LOCH d) он но OCH e) NH f)Select the best reagents to effect the given transformation. A a В b C D d HO а) 1) ВНз, THE 2) H2O2, NaOH b) 1) NABH4 2) H20 c) 1) Hg(OAc)2, H20 2) NABH4 d) Hг, Pd/C/hich of the following reagent best accomplish this transformation below? - CH=CH- -CEC- A (1st)Br2, CCI4, (2nd)2 NaNH2, NH3 B (1st) BH3, THF, (2nd) H2O2 (1st) H2, Lindlar, (2nd) H2O2 D (1st) HCI, (2nd) NaNH2, NH3
- QUESTION 6 Which set of reagents would best accomplish the transformation shown? O CH3CO3H O 1) 03 2) Zn, HCI O 1) B2H6 2) H202. Кон, Н20 O H20, H2SO4. HgSO4Draw the curved arrow mechanism for the following reaction. You must include all intermediates and the final products for this reaction. OH 1. BrMg-CH3 (2 equivs) 2. H H HFor the reaction shown, the major products form via the A) SN1 B) SN2 C) E1 D) E2 H₂, Br CH3CH₂OLi ©2017 ProtonGuru.com E) Mixture of E1 and E2 F) Mixture of S1 and SN2 G) Mixture of Sn2 and E2 H) Mixture of S1 and E1 1) No reaction pathway(s).
- 14. Provide the reagents necessary to complete the following transformation. CH₂CH3 A) 1. BH3 THF 2. H2O2, HO- B) H2O, H2SO4 C) Os04, H202 D) MMPP E) 1. MMPP 2. H+, H₂O CH₂CH3 OH ОН enantiomer8) What is the product of the reactions below? CH3CH2CH-CH2 CH3CO3H CH3OH, H2SO4(cat.) A) CH3CH₂CHCH₂OCH3 ОН B) CH3CH2CHCH2OH OCH3 C) CH3CH₂CHCH₂OH ОН D) CH3CH2CHCH2OH CH3 KWhat sequence of reagents would best achieve the transformation shown belon? Hr O 1) Br, FeBr 2) Fe, HCl 3) HNO, H SO, 1) Br,, FeBr, 2) HNO, H. SO,3) Fe, HCI 1) HNO,, H So, 2) Fe, HC1 3) Br,, FeBr, 1) HNO, H SO, 2) Br,, FeBr, 3) Fe, HCI
- 18) Which one of the following reaction steps work best to carry out the transformation shown below? OH A) 1) CH3I C) 1) CH3COOH B) K₂CO3 in Acetone, Butyl bromide D) 1) H₂SO4 2) CH3COOH 080.02. a. b. d. C. oFor each reaction, draw the product(s) and circle the mechanism(s). Include "major be and “minor" when necessary. Stereochemistry must be included for stereoselective reaction "No reaction" is a possible answer. Br Br ts Br CI ta ха но Br CH3ONa CH₂OH KSH acetone Br₂ hv CH3OH NaCN DMSO ser nongaholds zid) no baard E2 E1 SN1 SN2 X. E2 E1 SN1 SN2 X. E2 E1 SN1 SN2 X. E2 E1 SN1 SN2 X• E2 E1 SN1 SN2 X• E2 E1 SN1 SN2 X.2. The following transformations represent either a reversible or irreversible reaction with a carbonyl. In the box above each reaction arrow, specify whether the reaction is reversible "R" or irreversible "I". a. H. b. d. HO OH