I need the formation of acyl chloride then amide for the reaction below If you could...
If somebody could assist me with the below questions, I would greatly appreciate it! Thank you! 1. Discuss the trade-off between strength and ductility in design. For example, are there design situations where ductility would be more important than strength? 2. Is there any range of stress that can be applied to a material without appreciably altering some of its material properties? Explain. **I would really appreciate it if the answer could be typed!
I know the reactivity of carboxylic acid is acid halide > anhydride> ester > amide. "Recall that benzoyl chloride was slow to react with water, does this fit with the trend you just described? Why or why not?" So I think the answer to this statement should be it doesn't fit the trend. But could someone explain why?
I really need some help with part a and part b. if you
could also explain how you got to the answers that would be greatly
appreciated!! thank you!
GP-03. A block of mass 2.5 kg slides down a frictionless incline plane from rest as shown in figure below. At the bottom, it strikes another block of mass 7.0 kg, which is initially at rest. (a) find the velocity of the smaller block right after the collision, if the heavier...
I really need some help with #1 and 2 and if you could
also explain the steps I would greatly appreciate it!
1. Complete and balance each equation. Write the complete and the net ionic equations. If no reaction occurs, write "NO REACTION". a. Lil (aq) + Bas (aq) → b. KCl (aq) + Cas (aq) → C. CrBr2 (aq) + Na2CO3 (aq) → d. NaOH (aq) + FeCl3 → 2. Write a molecular equation for the precipitation reaction that...
I really need some help with number 3 and number 4 if
you could also explain the steps I would greatly appreciate it!
3. Write the complete and the net ionic equations for each acid-base reaction. a. HI (aq) + RbOH (aq) → b. HCHO2 (aq) + NaOH (aq) → C. HC2H302 (aq) + LiOH (aq) → 4. A 30.00-ml solution of H3PO4 of an unknown concentration is titrated with a 0.100 M NaOH solution. The equivalence point is reached...
If you could please answer 1,2ab,3ab and 4. I would greatly
appreciate it! Thank you.
What is a good source for broad-spectrum visible (and near IR) light? 12] 2. During a spectroscopy experiment, subjecting a sample to white light is often not a good idea. a. Why might white light irradiation be bad? [4] b. How does one avoid blasting a sample with full-spectrum light? 4] 3. Oxygen will react in something called the "Chapman Cycle" when exposed to short-wave...
I
need help with my biostatistics homework, if you could post what
formula you used I’d really appreciate it!
2. Look up the following t or P values: Format is ta[df] One-tailed critical value for t .01[14] - Answer: Two-tailed (right) critical value for t .05[17] - Answer: If ts=2.377 with 22 df, what is P for a 2-tailed hypothesis? Answer: If ts = 9.667 with 9 df, what is P for a 1-tailed hypothesis? Answer:
the first part is correct and so are the H+'s so i just need
help on the ester and acyl drawings please
Three reactions between a Grignard reagent and a carbonyl
compound are given below. Draw the main organic product for each
reaction and indicate if H or H%u2013 is needed to complete each
reaction. (The starting material structures are provided in the
answer fields as a starting point for your drawings.)
Could you please help and answer this question by drawing the
mechanism for the reaction and show a possible reaction condition
that would allow the product to be the only one forming? If you can
explain how and why that would be greatly appreciated. Thank
you!!
4. In place of the written protocol show the mechanism of the following reaction and determine how many products can form. Indicate the full mechanism for ONE product formation but show all potential final...
Could someone please explain how to do this. Thank you.
If you could explain in detail so I could understand I would
appreciate it very much!
Provide curved arrows to indicate the mechanism involved in each step of the following Hantzsch pyridine synthesis. 0 OH OH OH 0 он о O HO NH3 OH O H2N он он OH H