Having trouble finding R1,R2,R3,R4,R5,R6 any info would be awesome BJT Phase Shift Oscillator 12V VCC R3 R4 RC R1 Q2 C5 C8 R5 2N2222A C7 0.01HF 0.01HF 0.01 μF Q1 R7 C2 SineWave 2N2222A 22Ω Q-point R6 RE C4 100μF R2 lc 2ma Vce -5volts 12V VCC U1 JI LM7812CT LINE VOLTAGE VREG C3 470uF Title: FinalProject_Osc C1 0.1HF FinalProject_Osc Designed by. Dennis Leak Checked by Approved by. Document N 0001 Date: 2014-04-06 Sheet 1 Revision: 1.0 Size: A 1of...
Select the product for the following reaction: HO+H нон нон н +он CH,OH он ноо нонно он нон HO+H нон н+он н+он нон н он н +он нон нон н-он нон нон CH OH сн,он CH OH CH,OH 4 оооо
R1 R3 R5 N1 N3 N4 10 30 10 V1 R6 30 R4 R2 50 40 60 .op Answer the following questions: What is the current coming out of the power supply V1? What is the value of N1? What is the current through R2? What is the current through R6? 1) 2) 3) 4) 5) What is the power dissipated by R4? (HINT: Use Ps IR, or P WHAT TO TURN IN 1) 2) Cut and Paste of the...
A circuit made up of 6 resistors is shown in the figure, with resistances R1 = 16 Ω, R2 = 35 Ω, R3 = 29 Ω, R4 = 73 Ω, R5 = 89 Ω, and R6 = 31 Ω. The total current going through the circuit is I = 11.5 A. Part (a) Express the equivalent resistance of the combination of R4, R5, and R6. Part (b) Express the equivalent resistance of the combination of R3, R4, Rs and R6. Part (c) Express...
give the compund name HyC-CH2-C= н,с-сну-СН-СН со HC-он нус-сҢсна-он = HC-CH-C-OH
(10 points) 6. Circle all of the compounds below that are achiral OH сн, н Cl. OH на C H CI H CI CH снсн, CI H сHсH, Br (10 points) 7. Assign the absolute configuration of the stereooenters in each of the following compounds. NHg CH CHy-CH снон сн, COH H но снсH,B CHs Br HO CHCH Br CHy- он H- снсH
C=O 2. Which of the following is an example of an aldopentose? Circle your answer. СН,ОН CH,он CH н-с-он H-6-H H-C-OH HO-C-H. H-C-H H-C-OH H-C-OH H-6-H H-C-OH CH,OH CH,OH CH OH 3. In the L- isomer of a Fischer projection of a monosaccharide, the -OH group furthest from the carbonyl is written. Circle your answer. on the left of the top chiral carbon. on the left of the middle chiral carbon. on the left of the bottom chiral carbon. on...
4. Write out the 10 structure for the following polypeptide: он он HyN-CH-C-N-CH-C-N-CH-COO CH2 CH-OH CH C-NH2 CH3 COO 5. Illustrate the possible 2° structure interactions in the following polypeptide: R. 6. Identify the type of 3° structure interaction that will occur between the following pairs of amino acids: a) Aspartic acid and lysine b) Serine and tyrosine c) Leucine and valine d) Cysteine and cysteine 7. Draw out the products of the hydrolysis of the following polypeptide: HsN CH-C-N-C-C-N-C-C-N-CH-C-N-CH-COo...
NADP+ NADPHH HC-OH HO-CH HC-OH нс-ОН CH2OPO;? 6PGDH 'Coz CH OH c=0 HC-OH HC-OH CHOPO3 In pentose phosphate pathway, 6-phosphogluconate undergoes oxidation and decarboxylation by 6- phosphogluconate dehydrogenase (6PGDH) to form D-ribulose 5-phosphate. The reaction generates NADPH, as shown in the scheme. (1) Fill the blanks. During the 6PGDH-catalyzed reaction, the A group of carbon (B) of 6-phosphogluconate is oxidized to the group in ribulose 5-phosphate. A: (name of the functional group). B: (carbon numbering) C: (name of the functional...
3) Which of the following compounds is chiral? A) H Н-С-н н B) H HO C-OH Н C) CH3 HO-C-H Cl D) Br Н-С-ОН н E) C Br- C-C Br 4) In the L- isomer of a Fischer projection of a monosaccharide, the -OH group furthest from the carbonyl is written A) on the left of the top chiral carbon B) on the right of the top chiral carbon C) on the left of the middle chiral carbon D) on...