Explanation:
Dehydrohalogenation reactions occurs as elimination reactions through the following mechanism:
Step 1: A strong base(usually KOH) removes a slightly acidic hydrogen proton from the alkyl halide.
Step 2: The electrons from the broken hydrogen‐carbon bond are attracted toward the slightly positive carbon (carbocation) atom attached to the chlorine atom. As these electrons approach the second carbon, the halogen atom breaks free.
However, elimination will be slower in the exit of Hydrogen atom at the C2 and C3 because of the steric hindrance by the methyl group.
Elimination of the hydrogen from the methyl group is easier.
Thus, the major product will A
Answer:
eating
Explanation:
because when any food or anything that touches your saliva (spit) automatically a chemical reaction!
Answer: Theoretical Yield = 0.2952 g
Percentage Yield = 75.3%
Explanation:
Calculation of limiting reactant:
n-trans-cinnamic acid moles = (142mg/1000) / 148.16 = 9.584*10⁻⁴ mol
pyridium tribromide moles = (412mg/1000) / 319.82= 1.288*10⁻³ mol
- n-trans-cinnamic acid is the limiting reactant
The molar ratio according to the equation mentioned is equals to 1:1
The brominated product moles is also = 9.584*10⁻⁴ mol
Theoretical yield = (9.584*10⁻⁴ mol) * (Mr of brominated product)
= (9.584*10⁻⁴ mol) * (307.97) = 0.2952 g
Percentage Yield is : Actual Yield / Theoretical Yield = 0.2223/0.2952
= 75.3%
Answer:
hi! I'm pretty sure your answer is solvent!
Explanation:
not 100% sure but I looked it up on google. solvent does the dissolving, solute is what is being dissolved, and a solution is the solvent + the solute. hope this helped!
Answer:
I hope this will help you and Please mark me as Brilliant
Explanation:
Approximately 2 mL of Solution A (on the left) is added to a sample of Solution B (on the right) with a dropping pipet. If a precipitate forms, the resulting precipitate is suspended in the mixture. The mixture is then stirred with a glass stirring rod and the precipitate is allowed to settle for about a minute.
Solution A: 0.5 M sodium hydroxide, colorless
Solution B: 0.2 M nickel(II) nitrate, green
Precipitate: light green
Ni(NO3)2(aq) + 2 NaOH(aq) —> Ni(OH)2(s) + 2 NaNO3(aq)
Credits:
Design
Kenneth R. Magnell Central Michigan University, Mt. Pleasant, MI 48859
John W. Moore University of Wisconsin - Madison, Madison, WI 53706
Video
Jerrold J. Jacobsen University of Wisconsin - Madison, Madison, WI 53706
Text
Kenneth R. Magnell Central Michigan University, Mt. Pleasant, MI 48859
