(a) he reagent(s) type yo Choose the reagents from the ones shown below (A-L). E للہ علہلہ پہلا میں مللی پھیلہ میر رہی ہلو بلی میر بلد Br F prepare Tollowing target Br Br C G K
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Q: I need help with these problem...
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Formation of beta keto ester
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- Please answer both part A and B as it belongs to same question. ThankyouSelect the keyword or phrase that will best complete each sentence. Key terms: Toluene reacts faster than benzene in all substitution reactions. Thus, its electron- CH, group the benzene ring to acid electrophilic attack. activates A resonance effect is electron when resonance structures place a negative charge on carbons of the benzene ring. base k deactivates Inductive effects stem from the of the atoms in the substituent and the of the substituent groups. donating In a Friedel-Crafts alkylation, benzene is treated with an alkyl halide and a Lewis donation (AICI) to form an alkyl benzene. electronegativity nces When a neutral O or N atom is bonded directly to a benzene ring, the effect dominates and the net effect is electron inductive polarizability Nitrobenzene reacts more slowly than benzene in all substitution reactions. Thus, NO, group its electron- the benzene ring. poor A resonance effect is electron positive charge on carbons of the benzene ring. resonance when resonance…Reposting please solve it correctly!!! I'll Upvote you please help me !!!
- 29 minutes, 42 seconds. Question Completion Status: A Moving to another question will save this response. Question 15 What is not an expected product of the following allylic substitution reaction? NBS, hv Br Br Compounds II and II Compound II only O Compound I only O Compound II only A Moving to another question will save this response O O Cif Therapeutic index increase,does it means that it cause higher death rate??The next set of questions are assertion type: There are two statements in a sentence. Choose from the options A-E if A. Both statements are true and related B. Both statements are true but not related C. The first statement is true and the second statement is false D. The first statement is false and the second statement is true E. Both statements are false Benzylamine synthesis from benzaldehyde follows the mechanism of reductive amination BECAUSEbenzylamine is synthesised form benzaldehyde through an enamine intermediate Hyperconjugation can stabilise carbocation intermediates BECAUSE secbutyl carbocation can rearrange to a tertbutyl carbocation. Reductive amination requires a hydrogen on the carbonyl carbon to proceed BECAUSE Reductive amination converts only aldehydes to amines
- Draw the organic product of the reactionHello, I do not understand these questions for chemistry and I am stuck. May I get help please please?? An explanation leading to steps would be helpful. Thank you. Question: Draw the MAJOR organic product(s) for the following reactions. If no reaction occurs state no reaction in the box provided.Unanswered A Su Pre-lab question 3 Homework Unanswered The borohydride reduction of a ketone involves a nucleophilic attack on the electrophilic ketone carbon. The attacking nucleophile is? Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. The boron atom of sodium borohydride. The hydrogen atom (acting as a hydride) of the sodium borohydride. The hydrogen atom (acting as a proton) of the sodium borohydride. The sodium atom of sodium borohydride. Show MacBook Pro P.
- I only need help with questions three, please solve but always explain. I am not sure what the question is asking, and no other techniques come to mind when thinking about how to dry crystals more.Do all and label question with answers so I know thank youPredict the missing product of this organic reaction please: