Can you explain how to get this answer? I’m confused on how to get this specific...
Really confused about this problem.Please tell me the answer as specific as possible!Thanks! The following addition reaction will proceed when bromine forms two radicals via homolytic cleavage. The radicals then react with ethene to form which product? HH C=C + Brz
Really confused about this problem.Please tell me the answer as specific as possible!Thanks! The following addition reaction will proceed when bromine forms two radicals via homolytic cleavage. The radicals then react with ethene to form which product? =C + Br2 Br
Im confused how the answer is formed from the given chemical structure. Can you explain step by step what to do? What is the carbon chain product of the elimination reaction beginning with the reactant shown below? Br Hint: the eliminated product is HBr. What is left? CHBr=CHBr CH2Br–CH2Br HC=CH H2C=CH2
Can you help me answer these 5 questions please 1. How many total valence electrons will there be on the PO43- ion (a -3 ion)? 2. How many lone pairs of electrons are on the entire structure in the correct Lewis structure for CS2 ? 3. How many lone pairs of electrons will be on the central atom in the correct Lewis structure for PBr5? 4. Which fo the following atoms can have an expanded octet? A. S B. O...
can you explain in detail how to get this answer , like any math or idea/concepts please be specific ! 10, CH Br2 (hint: Br-81:Br-71:1) Ratio for 172.174176 molecularions is L21 Ratio for 172:174:176 molecular ions is
3. Based on your answer in 2. select the most likely reaction pathway. Explain how the substitution mechanism forms the product structure(s) shown. 2points А, H Br off and add NH toi O position because it Would Rick Ph Ph Ph- B H NH2 Ph Ph + NH 4. Identify the reaction components and solvents as more soluble in the aqueous (A) or organic (O) layer during separation of substitution and protonation steps. 3 pts Br HN НN CIO NH3...
How do you get the answer just a little confused Version 1 12. Methyl red is a common acid-base indicator. It has a Ka equal to 6.3 x 10-. Its un-ionized form 7.82 is red and its anionic form is yellow. What color would a methyl red solution have at pH A) violet B) yellow C) green D) blue E) red 13 Assuming egual concentrations of conllgate hase and acid uhich one of tho f uolu, n a
can questions 1-9 please be answered and why are they the answer 1. How many sp hybridized carbon atoms are present in the following molecule? (A) 3 (B) 4 5 н.с (D). 6 2. Which bond is the longest in the following molecule? (A) (B) CECH (C) (D) 3. Which of the following molecules is chiral at room tempernture (25 C)? (A) 1,1-dimethylcyclohexane (B) cis-1,2-dimethyleyelohexanc (C) trans-,3-dimethyleyclohexane (D) trans-1,4-dimethylcyclohexane 4. Which group is an aldehyde? н н (C) (D) (A)...
Explain why dimethyl maleate is converted in high yield to dimethyl fumarate under the conditions you used. Use thermodynamic and kinetic arguments to justify your answer. How does the reaction preformed relate to the isomerization of retinal in the human eye (which enables vision). Primer: A major topic covered in the second half of Organic I is the properties and reactivity of alkenes. This lab experiment will provide you with an opportunity to examine alkene reactivity by conducting an isomerization...
please answer the prelab excercise:) I tried doing it but I did not get very far Experiment 7: Grignard Reaction. Introduction Discovered by French chemist Victor Grignard, the reaction that now bears his name is an example of the preparation of an organometallic reagent. In this lab, phenylmagnesium bromide is the Grignard of interest, and it will be added to an aldehyde to produce an alcohol. Lab Objectives 1. To study organometallic reagents in general. benzophenone. 2. To prepare phenylmagnesium...