Answer: genotype: Ee phenotype: two small eyes.
genotype: RR' phenotype: pink eyes
genotype: GB phenotype: green and blue splotches
genotype: cc phenotype: straight
genotype: Tt phenotype: has tail
genotype: Ss phenotype: sharp teeth
genotype: FF' phenotype: three toes
genotype: ww phenotype: white
genotype: YY phenotype: pointy
genotype: nn phenotype: two ears
genotype: Ll phenotype: long
Explanation: hope this helps (the uppercase letters are dominant genes. the lowercase letter are recessive genes. for a recessive gene to show up in a phenotype you need 2 lower case letters such as cc or ss. for a dominant gene to show up in phenotype you need either 1 or 2 uppercase letters such as Cc or SS. Codominant genes present both colors in the phenotypes i.e. a brown and white cow. incomplete dominance is when neither gene is dominant so a mix of the 2 are present in the phenotype i.e. a pink rose. A regulatory gene controls the expression of a gene
Answer:
5.0 moles of water per one mole of anhydrate
Explanation:
To solve this question we must find the moles of the anhydrate. The difference in mass between the dry and the anhydrate gives the mass of water. Thus, we can find the moles of water and the moles of water per mole of anhydrate:
<em>Moles Anhydrate:</em>
7.58g * (1mol / 84.32g) = 0.0899 moles XCO3
<em>Moles water:</em>
15.67g - 7.58g = 8.09g * (1mol / 18.01g) = 0.449 moles H2O
Moles of water per mole of anhydrate:
0.449 moles H2O / 0.0899 moles XCO3 =
5.0 moles of water per one mole of anhydrate
You are right, it's CA Calcium, 40.08, Group 2 and Row 4.
The concentrations : 0.15 M
pH=11.21
<h3>Further explanation</h3>
The ionization of ammonia in water :
NH₃+H₂O⇒NH₄OH
NH₃+H₂O⇒NH₄⁺ + OH⁻
The concentrations of all species present in the solution = 0.15 M
Kb=1.8 x 10⁻⁵
M=0.15
![\tt [OH^-]=\sqrt{Kb.M}\\\\(OH^-]=\sqrt{1.8\times 10^{-5}\times 0.15}\\\\(OH^-]=\sqrt{2.7\times 10^{-6}}=1.64\times 10^{-3}](https://tex.z-dn.net/?f=%5Ctt%20%5BOH%5E-%5D%3D%5Csqrt%7BKb.M%7D%5C%5C%5C%5C%28OH%5E-%5D%3D%5Csqrt%7B1.8%5Ctimes%2010%5E%7B-5%7D%5Ctimes%200.15%7D%5C%5C%5C%5C%28OH%5E-%5D%3D%5Csqrt%7B2.7%5Ctimes%2010%5E%7B-6%7D%7D%3D1.64%5Ctimes%2010%5E%7B-3%7D)
![\tt pOH=-log[OH^-]\\\\pOH=3-log~1.64=2.79\\\\pH=14-2.79=11.21](https://tex.z-dn.net/?f=%5Ctt%20pOH%3D-log%5BOH%5E-%5D%5C%5C%5C%5CpOH%3D3-log~1.64%3D2.79%5C%5C%5C%5CpH%3D14-2.79%3D11.21)
Answer:
Here's what I get
Explanation:
(a) Intermediates
The three structures below represent one contributor to the resonance-stabilized intermediate, in which the lone pair electrons on the heteroatom are participating (the + charge on the heteroatoms do not show up very well).
(b) Relative Stabilities
The relative stabilities decrease in the order shown.
N is more basic than O, so NH₂ is the best electron donating group (EDG) and will best stabilize the positive charge in the ring. However, the lone pair electrons on the N in acetanilide are also involved in resonance with the carbonyl group, so they are not as available for stabilization of the ring.
(c) Relative reactivities
The relative reactivities would be
C₆H₅-NH₂ > C₆H₅-OCH₃ > C₆H₅-NHCOCH₃
